Identity
- Trade Name
- Aesculap EUDAMEDFDA UDI
- Generic Name
- Manual surgical saw, rigid FDA UDI
- Device Name
- Nasal saw EUDAMEDJOSEPH NASAL SAW BAYO LFT-CVD 170MM FDA UDI
- Model / Reference
- OL452R EUDAMEDFDA UDI
- Description
- JOSEPH NASAL SAW BAYO LFT-CVD 170MM FDA UDI
Identifiers
- Catalog Number
- OL452R FDA UDI
- Primary DI / UDI-DI
- 04038653178612 EUDAMEDFDA UDI
- Basic UDI-DI
- 4039239000001306ZW EUDAMED
- Direct Marketing DI
- 04038653178612 EUDAMED
- FDA Product Code
- KBC FDA UDI
- EMDN Code
- L010701 MANUAL SURGICAL SAWS, REUSABLE EUDAMED
- GMDN Term
- Manual surgical saw, rigid FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 874.4420 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
Aesculap 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 | 4039239000001306ZW | 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 75a2a960-8a42-4668-ac4a-4bec24f5b546 61 fields · synced Jul 9, 2026
- FDA UDI 92a90e6f-6968-4664-b2d6-9a6e67bc6dfe 35 fields · synced May 30, 2026