Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Manual surgical saw, rigid FDA UDI
- Device Name
- SPARE BLADE F/FO900R FDA UDI
- Model / Reference
- FO901R FDA UDI
- Description
- SPARE BLADE F/FO900R FDA UDI
Identifiers
- Catalog Number
- FO901R FDA UDI
- Primary DI / UDI-DI
- 04038653169580 FDA UDI
- FDA Product Code
- GDR FDA UDI
- GMDN Term
- Manual surgical saw, rigid FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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: Manual surgical saw, rigid
Aesculap by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Manual surgical saw, rigid.
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- LINDEMANN AMPUTATION SAW — SONTEC INSTRUMENTS, INC. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- V. Mueller — STERIS CORPORATION · Class I
- Intramedullary Bone Saw — Biomet Orthopedics, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI f6eaafac-ac4e-4397-8c6c-d75044fe57cc 35 fields · synced May 30, 2026