Identity
- Trade Name
- BAYONET SPINAL KNIFE HANDLE FDA UDI
- Generic Name
- Haemostatic knife FDA UDI
- Device Name
- BAYONET SPINAL KNIFE HANDLE #3 FDA UDI
- Model / Reference
- 400-428 FDA UDI
- Description
- BAYONET SPINAL KNIFE HANDLE #3 FDA UDI
Identifiers
- Catalog Number
- 400-428 FDA UDI
- Primary DI / UDI-DI
- 00192896078567 FDA UDI
- FDA Product Code
- GDZ FDA UDI
- GMDN Term
- Haemostatic knife 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
Dimensions & Sizes
- Size
- Length — 13.75 Inch FDA UDI
Category: Haemostatic knife
Bayonet Spinal Knife Handle by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Haemostatic knife.
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- HEMOSTATIX THERMAL SCALPEL SYSTEM MODEL P8400 CONTROLLER — HEMOSTATIX MEDICAL TECHNOLOGIES LLC · Class II
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
- Sontec Instruments, Inc.
Sources (1)
- FDA UDI 7777e7ee-65e2-4d36-8c9d-3664e43dff75 36 fields · synced May 31, 2026