Identity
- Trade Name
- DUROTIP® EUDAMEDDUROTIP FDA UDI
- Generic Name
- General-purpose surgical scissors, reusable FDA UDI
- Device Name
- Ring scissors Ir EUDAMEDMETZENBAUM DUROTIP TC Dissecting Scissors, curved, 7", (180 mm), blunt/blunt, non-sterile, reusable FDA UDI
- Model / Reference
- BC263R EUDAMEDFDA UDI
- Description
- METZENBAUM DUROTIP TC Dissecting Scissors, curved, 7", (180 mm), blunt/blunt, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- BC263R FDA UDI
- Primary DI / UDI-DI
- 04038653137817 EUDAMEDFDA UDI
- Basic UDI-DI
- 403923900000062023 EUDAMED
- Direct Marketing DI
- 04038653137817 EUDAMED
- FDA Product Code
- LRW FDA UDI
- EMDN Code
- L010403 SURGICAL DISSECTION SCISSORS, REUSABLE EUDAMED
- GMDN Term
- General-purpose surgical scissors, 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
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
Yes
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: General-purpose surgical scissors, reusable
Durotip® by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Also classified as General-purpose surgical scissors, reusable.
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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 | 403923900000062023 | 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 1671f18d-f33b-4686-a1dd-1b4dee05431e 61 fields · synced Jun 18, 2026
- FDA UDI 38a857e0-011b-4c5d-9428-2f280063b90e 35 fields · synced May 30, 2026