Identity
- Trade Name
- Aesculap EUDAMEDFDA UDI
- Generic Name
- Nail clippers, reusable FDA UDI
- Device Name
- Nail and cuticle nipper EUDAMEDNail Forceps, 5 1/4", (135 mm), non-sterile, reusable FDA UDI
- Model / Reference
- HF211R EUDAMEDFDA UDI
- Description
- Nail Forceps, 5 1/4", (135 mm), non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- HF211R FDA UDI
- Primary DI / UDI-DI
- 04038653049363 EUDAMEDFDA UDI
- Basic UDI-DI
- 403923900000069634 EUDAMED
- Direct Marketing DI
- 04038653049363 EUDAMED
- FDA Product Code
- FZT FDA UDI
- EMDN Code
- L0199 SHARP INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Nail clippers, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 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
Category: Nail scissors, reusable
Aesculap by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Also classified as Nail scissors, reusable.
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- LIGHTED SHORT TOOTH BLADE, 14 X 120MM — TeDan Surgical Innovations, Inc. · Class IIa
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 | 403923900000069634 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED e8ee116c-c4b0-484f-b762-2ef46fa4670f 61 fields · synced Jul 10, 2026
- FDA UDI 81be88b9-f068-4476-a3d6-d45796fc7feb 35 fields · synced May 30, 2026