Identity
- Trade Name
- YASARGIL ARACHNOID KNIFE FDA UDI
- Generic Name
- Haemostatic knife FDA UDI
- Device Name
- YASARGIL ARACHNOID KNIFE PARTIAL CURVED BLADE FDA UDI
- Model / Reference
- 400-427 FDA UDI
- Description
- YASARGIL ARACHNOID KNIFE PARTIAL CURVED BLADE FDA UDI
Identifiers
- Catalog Number
- 400-427 FDA UDI
- Primary DI / UDI-DI
- 00192896033061 FDA UDI
- FDA Product Code
- EMF 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 — 7.25 Inch FDA UDI
Category: Haemostatic knife
Yasargil Arachnoid Knife by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Haemostatic knife.
- HEMOSTATIX THERMAL SCALPEL SYSTEM MODEL P8400 FOOTSWITCH — HEMOSTATIX MEDICAL TECHNOLOGIES LLC · Class II
- TREPHINE — KLS-Martin L.P. · Class I
- SHAW SCALPEL — C2DX, INC. · Class II
- SHAW SCALPEL — C2DX, INC. · Class II
- HEMOSTATIX THERMAL SCALPEL SYSTEM MODEL 5812 BLADE — HEMOSTATIX MEDICAL TECHNOLOGIES LLC · Class II
- HEMOSTATIX THERMAL SCALPEL SYSTEM MODEL 5715 BLADE - QTY 24 — HEMOSTATIX MEDICAL TECHNOLOGIES LLC · Class II
- HEMOSTATIX THERMAL SCALPEL SYSTEM MODEL 5710 BLADE - QTY 24 — HEMOSTATIX MEDICAL TECHNOLOGIES LLC · Class II
- 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sontec Instruments, Inc.
Sources (1)
- FDA UDI 74f0ed7d-2ad1-4939-bd7a-399a0360a1cb 36 fields · synced Jun 8, 2026