Identity
- Trade Name
- MOPYLEN FDA UDI
- Generic Name
- Polyolefin/fluoropolymer suture, monofilament FDA UDI
- Model / Reference
- MOPYLEN FDA UDI
Identifiers
- Primary DI / UDI-DI
- E203US71415 FDA UDIE203US70240 FDA UDIE203US7156 FDA UDIE203US70712 FDA UDI
- 510(k) Number
- K143582 FDA UDI
- FDA Product Code
- GAW FDA UDI
- GMDN Term
- Polyolefin/fluoropolymer suture, monofilament FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5010 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDIFDA UDI
Category: Polyolefin/fluoropolymer suture, monofilament
Mopylen by Resorba Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Polyolefin/fluoropolymer suture, monofilament.
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- ATRAMAT — Internacional Farmacéutica S.A DE C.V · Class II
- DemeLENE — DemeTECH Corp · Class II
- WEGO-Polypropylene Nonabsorbable Surgical Suture With Needle — Foosin Medical Supplies, Inc. · Class II
- Premilene — B BRAUN SURGICAL SA · Class II
- DEKNATEL — TELEFLEX INCORPORATED · Class II
Cleared under the same submission
K143582 also covers:
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
- MOPYLEN — Resorba Medical GmbH
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Resorba Medical GmbH
Sources (4)
- FDA UDI 4ff1aec5-f545-4df2-8238-cec6e2497f7e 33 fields · synced May 31, 2026
- FDA UDI f15d2c57-89dd-437c-aa86-c2014781cf7e 33 fields · synced May 26, 2026
- FDA UDI cdf18b57-07cf-479c-9544-cac63ccc749c 33 fields · synced May 27, 2026
- FDA UDI 82fede76-5437-432c-b28a-324fa32b1d55 33 fields · synced May 27, 2026