Identity
- Trade Name
- ERGOPLANT EUDAMEDFDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Tweezers I EUDAMEDERGOPLANT Dental Tissue Forceps, straight, 4 3/4", (120 mm), non-sterile, reusable FDA UDI
- Model / Reference
- DX051R EUDAMEDFDA UDI
- Description
- ERGOPLANT Dental Tissue Forceps, straight, 4 3/4", (120 mm), non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- DX051R FDA UDI
- Primary DI / UDI-DI
- 04038653385713 EUDAMEDFDA UDI
- Basic UDI-DI
- 403923900000054024 EUDAMED
- Direct Marketing DI
- 04038653385713 EUDAMED
- FDA Product Code
- EMH FDA UDI
- EMDN Code
- L031308 SURGICAL AND ANATOMICAL TWEEZERS, REUSABLE EUDAMED
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Ergoplant by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 403923900000054024 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED 3a8f8b79-d3cc-4e77-b169-08f2f9b23853 61 fields · synced Jun 18, 2026
- FDA UDI 4ad324f8-2b17-4dc5-b0fc-3196a87f8490 35 fields · synced May 29, 2026