Identity
- Trade Name
- ERGOPERIO EUDAMEDAESCULAP FDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- Spoon EUDAMEDHEMINGWAY Bone Curette, angled, 6 3/4", (170 mm), double ended, sharp/sharp, Fig. 3, non-sterile, reusable FDA UDI
- Model / Reference
- DO673R EUDAMEDFDA UDI
- Description
- HEMINGWAY Bone Curette, angled, 6 3/4", (170 mm), double ended, sharp/sharp, Fig. 3, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- DO673R FDA UDI
- Primary DI / UDI-DI
- 04038653037537 EUDAMEDFDA UDI
- Basic UDI-DI
- 403923900000040823 EUDAMED
- FDA Product Code
- EMK FDA UDI
- EMDN Code
- L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED
- GMDN Term
- Bone curette, 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
Yes
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 | 403923900000040823 | 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 ed2f9f56-59ce-47d4-84ab-b98d70aec9bf 61 fields · synced Jun 18, 2026
- FDA UDI f1a80816-9070-4c82-b17b-24f4cce6c005 35 fields · synced May 30, 2026