--- schema: "waleerat.service-markdown/v2" id: "service:ultracol" kind: "service" locale: "de" requested_lang: "de" lang: "de" translation_state: "localized" translation_group: "service:ultracol" title: "Ultracol Program" family: "injectable" status: "released" canonical_html: "https://waleeratclinic.com/de/ultracol" resource_uri: "https://waleeratclinic.com/markdown/de/ultracol" content_version: "2026-08-30.2" modified: "2026-08-30" content_hash: "sha256:a8cb0620137a7c11e5756471eee53078b747c0e7643df7b54bc295376effa7bb" source_checked: "Quellen geprüft 27 August 2026" source_set: - "https://www.ultracol.com/en/" - "https://doi.org/10.3390/cosmetics11010004" - "https://en.fda.moph.go.th/entrepreneurs-medical-devices/category/for-commercial-purpose" price_ref: null claim_policy: "same reviewed SSOT as visible HTML; no patient-specific diagnosis or recommendation" tools: - "list_released_services" - "get_service_detail" - "get_service_section" - "compare_service_facts" - "get_service_price" - "start_booking_handoff" - "list_media_assets" - "get_media_asset" detail_level: "expanded" publication_scope: "general information; not diagnosis or individual treatment advice" --- # Ultracol Program A consultation-led page for people comparing injectable options. The exact product variant, treatment area, amount, session plan, risks, alternatives and current itemised quotation must be confirmed before treatment. > General information only. It is not a diagnosis or a recommendation for treatment. Suitability and response vary. ## Übersicht ### Was ist Ultracol Program? Ultracol Program is a medical-device product based on biodegradable PDO (polydioxanone) microspheres. The manufacturer's current public information describes a Korea MFDS-approved indication for temporary improvement of bilateral nasolabial folds. The exact product variant, planned area, amount and local product documentation used at Waleerat Clinic must be verified during consultation. Ultracol Program is not PDRN, salmon-derived material or an HA filler. ## Übersicht - **Termin:** Unterschiedlich je nach Bereich und Individuum - **Erholung:** Tägliche Aktivität ist oft möglich; Reaktion variiert - **Komfort:** Unbehagen variiert je nach Bereich und Hautzustand - **Material:** PDO Mikrokügelchen; prüfen Sie die genaue Variante ## Die Fragen, die diese Entscheidung ändern. ### Ist Ultracol Program PDRN oder aus Lachs hergestellt? No. The current manufacturer information identifies the product material as PDO (polydioxanone) microspheres. Ask the clinic to show the exact variant and local product documentation because similar-sounding injectable names are not interchangeable. ### Was ist der Unterschied zwischen Ultracol Program 100 und Ultracol Program 200? The currently verified public manufacturer page does not provide a complete side-by-side instructions-for-use comparison. Do not infer that the variants are interchangeable from a product name or online image. Confirm the sealed variant, local label, intended area, amount and current instructions for use before deciding. ### Wie viele Ultracol Program-Sitzungen sind erforderlich? A 2024 study of 31 adults with nasolabial folds used two ULTRACOL100 applications four weeks apart. That small, short study protocol is not a universal schedule for every variant, area or person. The session plan should follow assessment, the exact product documentation and review of response. ### Wann werden Veränderungen bewertet und wie lange halten sie sich? The 2024 ULTRACOL100 study assessed participants four weeks after each application and followed the two-session protocol for eight weeks. It therefore does not establish a universal long-term duration. Agree on a review point and avoid treating an old promotional duration as a guarantee. ### Ist Ultracol Program für den Unter Augenbereich etabliert? The manufacturer’s current public English page states a Korea MFDS-approved indication for temporary improvement of bilateral nasolabial folds. The verified source set used for this page does not establish an under-eye indication. Under-eye concerns, previous procedures and alternatives need a separate physician assessment. ### Was zeigen die aktuellen Sicherheitsdaten? In the 31-person ULTRACOL100 study, no participant withdrew early because of a treatment-related adverse effect during the short follow-up. The authors also identified the small sample and short follow-up as limitations and called for larger and longer safety evaluation. This is not proof that uncommon or long-term complications cannot occur. ### Was sollte ich vor dem Vergleich von Ultracol Program mit Filler oder einem anderen Injektionsmittel offenlegen? Share prior procedures in the area, medicines and supplements, allergies, health conditions, pregnancy or breastfeeding, future surgery plans and any important travel or event date. The verified evidence does not support one universal sequence with filler or other injectables; the comparison must be individualized. ### Wie ist der Ultracol Program-Preis im Vergleich zu Alternativen? Use a current itemised quotation that names the exact product and variant, vial or quantity basis, area, physician fee, comfort plan, aftercare and follow-up. A headline price cannot be compared fairly when the product, amount or plan differs. ## Compare the exact product, amount and treatment plan. An injectable name alone does not establish composition, amount, area, sessions, recovery or suitability. ### Country + exact product Confirm manufacturer, country, product family, exact variant and material or active component. Ask how product identity is checked. ### Area + quantity + purpose Compare the planned area, syringe or vial basis, amount, intended purpose and alternatives. Do not compare a single headline price across different plans. ### Sessions + risks + follow-up Confirm session plan, review timing, common and important risks, written aftercare, urgent contact route and what is included in the quotation. > Confirm the manufacturer country and exact product variant from the clinic before treatment. ## Die dienstspezifische Grenze zur Bestätigung. Prüfen Sie das versiegelte Produkt, die genaue Variante, den Chargenvermerk, das Verfallsdatum, das lokale Etikett und die Gebrauchsanweisung vor der Behandlung. Verlassen Sie sich nicht auf ein Online-Foto zur Bestätigung der Echtheit und verwenden Sie keine veralteten Beschreibungen von PDRN oder salmonabgeleiteten Produkten für Ultracol Program. ## Fragen, bevor Sie sich entscheiden. ### Können internationale Besucher vor der Reise eine Beratung erhalten? Ja. Teilen Sie Ihre bevorzugte Sprache und Reisepläne über einen internationalen Kontaktkanal mit. Bestätigen Sie Terminzeitpunkt, Materialanforderungen und Nachsorgevereinbarungen vor der Reise. ## Offizielle Quellen - [ULTRACOL amtliche Produktinformationen](https://www.ultracol.com/en/) - [Trinh et al. 2024 ULTRACOL100 nasolabial-fold study](https://doi.org/10.3390/cosmetics11010004) - [Thailändische FDA-Medizinprodukte-Werbung und Verifizierungsanforderungen](https://en.fda.moph.go.th/entrepreneurs-medical-devices/category/for-commercial-purpose) Quellen geprüft 27 August 2026 ## Beratung - [LINE](https://line.me/R/ti/p/@waleerat) - [WhatsApp](https://wa.me/66944512244) - [Messenger](https://m.me/waleeratclinic) - [Instagram DM](https://ig.me/m/waleerat_international_clinic) - [Anrufen](tel:+66927896699) Messaging is not monitored as an emergency service. Language availability and response times can vary. ## Machine-readable relationship - HTML canonical: https://waleeratclinic.com/de/ultracol - Markdown twin: https://waleeratclinic.com/markdown/de/ultracol - Discovery index: https://waleeratclinic.com/sitemap-md.txt