Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Aneurysm clip applier FDA UDI
- Device Name
- STD SLIM TI CLIP APPLIER 50MMX20DEG UP FDA UDI
- Model / Reference
- TEK7036R FDA UDI
- Description
- STD SLIM TI CLIP APPLIER 50MMX20DEG UP FDA UDI
Identifiers
- Catalog Number
- TEK7036R FDA UDI
- Primary DI / UDI-DI
- 04046955823352 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
- 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
MR Unsafe FDA UDI
Category: Aneurysm clip applier
Aesculap by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI ead170dc-e46c-4a33-bd59-18eb35875f58 35 fields · synced May 30, 2026