Identity
- Trade Name
- FEATHER MICROTOME BLADE FDA UDI
- Generic Name
- Microtome blade IVD, reusable FDA UDI
- Model / Reference
- A-22 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04902470058269 FDA UDI
- FDA Product Code
- IDL FDA UDI
- GMDN Term
- Microtome blade IVD, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3010 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Category: Microtome blade IVD, reusable
Feather Microtome Blade by Feather Safety Razor Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Microtome blade IVD, reusable.
- Tissue-Tek® Feather® — Sakura Finetek USA, Inc · Class I
- Accu-Cut® SRM™ 200 — Sakura Finetek USA, Inc · Class I
- Epredia — Richard-Allan Scientific LLC · Class I
- Tissue-Tek® Feather® — Sakura Finetek USA, Inc · Class I
- Epredia — Richard-Allan Scientific LLC · Class I
- Epredia — Richard-Allan Scientific LLC · Class I
- Epredia — Richard-Allan Scientific LLC · Class I
- Accu-Edge® — Sakura Finetek USA, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Feather Safety Razor Co., Ltd.
Sources (1)
- FDA UDI 2bf22c76-b16f-4c0c-b740-aa02771376b4 32 fields · synced Jun 8, 2026