Identity
- Trade Name
- ERGOPERIO EUDAMEDFDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Tweezers I EUDAMEDERGOPERIO Dressing Forceps (Tweezers), curved, 6 7/8", (175 mm), round handle, non-sterile, reusable FDA UDI
- Model / Reference
- DX061R EUDAMEDFDA UDI
- Description
- ERGOPERIO Dressing Forceps (Tweezers), curved, 6 7/8", (175 mm), round handle, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- DX061R FDA UDI
- Primary DI / UDI-DI
- 04046964540080 EUDAMEDFDA UDI
- Basic UDI-DI
- 403923900000054024 EUDAMED
- Direct Marketing DI
- 04046964540080 EUDAMED
- FDA Product Code
- EMG 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
Ergoperio 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 e4dd62cb-9040-484d-9c1d-eaffc4a23b6e 61 fields · synced Jun 19, 2026
- FDA UDI 487e3c5c-82dd-467c-85c9-62ab6478fa32 35 fields · synced May 30, 2026