Identity
- Trade Name
- Tissue-Tek® Accu-Edge® FDA UDI
- Generic Name
- Manual scalpel blade, reusable FDA UDI
- Device Name
- Trimming Blade, Long (10 inches); 50/case FDA UDI
- Model / Reference
- 4789 FDA UDI
- Description
- Trimming Blade, Long (10 inches); 50/case FDA UDI
Identifiers
- Catalog Number
- 4789 FDA UDI
- Primary DI / UDI-DI
- 14902470068883 FDA UDI
- FDA Product Code
- JOK FDA UDI
- GMDN Term
- Manual scalpel blade, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6820 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
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Manual scalpel blade, reusable
Tissue-Tek Accu-Edge Manual Scalpel Blade is a reusable, high-grade stainless steel device designed for precision cutting and dissection of tissues in surgical procedures. With its interchangeable handle and accurate cutting edge, this scalpel blade is ideal for various medical specialties.
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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
- Sakura Finetek USA, Inc
Sources (1)
- FDA UDI 85ea4b4e-c7f0-4270-a4a6-163d5e5c67b7 35 fields · synced Jul 21, 2026