Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Aneurysm clip applier FDA UDI
- Device Name
- YASARGIL Clip Applier Forceps, bayonet, 9 3/4", (245 mm), working length: 4 3/8", (110 mm), bayonet-shaped, without ratchet, mini, stainless steel, non-sterile, reusable FDA UDI
- Model / Reference
- FE316K FDA UDI
- Description
- YASARGIL Clip Applier Forceps, bayonet, 9 3/4", (245 mm), working length: 4 3/8", (110 mm), bayonet-shaped, without ratchet, mini, stainless steel, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- FE316K FDA UDI
- Primary DI / UDI-DI
- 04046963469559 FDA UDI
- FDA Product Code
- HCI FDA UDI
- GMDN Term
- Aneurysm clip applier FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4175 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Aesculap by Aesculap, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI 2061c291-f49a-4c2a-9c80-cb17c4a81c7d 36 fields · synced Jun 6, 2026