Identity
- Trade Name
- De Soutter Medical FDA UDI
- Generic Name
- Surgical saw blade, sagittal, reusable FDA UDI
- Device Name
- TPLO BLADE - SLOCUM - RADIUS 27MM FDA UDI
- Model / Reference
- 20120 FDA UDI
- Description
- TPLO BLADE - SLOCUM - RADIUS 27MM FDA UDI
Identifiers
- Catalog Number
- 20120 FDA UDI
- Primary DI / UDI-DI
- 05051471193116 FDA UDI
- FDA Product Code
- GEY FDA UDI
- GMDN Term
- Surgical saw blade, sagittal, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
De Soutter Medical by De Soutter Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- De Soutter Medical, Ltd.
Sources (1)
- FDA UDI 5d40a26f-905c-470d-8640-d5ee971fc0db 35 fields · synced Jun 8, 2026