Identity
- Trade Name
- ProDerm ULTRA 2 EUDAMED
- Device Name
- ProDerm ULTRA 2 EUDAMED
- Model / Reference
- BPLN-30BC EUDAMEDBPLN-30JC EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08809947983269 EUDAMED08809947983092 EUDAMED
- Basic UDI-DI
- B-08809947983269 EUDAMEDB-08809947983092 EUDAMED
- EMDN Code
- P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Türkiye EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
ProDerm ULTRA 2 by BioPlus Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08809947983269 | Class III | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- BioPlus Co., Ltd.
- EUDAMED SRN
- KR-MF-000008618
- Authorised Representative
- KTR Europe GmbH DE-AR-000005685
Sources (2)
- EUDAMED e357fa4e-8844-41d6-bdea-b0218172d4a7 61 fields · synced Jul 26, 2026
- EUDAMED 24aa0069-c961-421d-ac95-78958576d572 61 fields · synced May 18, 2026