Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
- Device Name
- YASARGIL Bipolar Forceps, straight, 9 1/4", (235 mm), working length: 4 1/2", (115 mm), bayonet-shaped, ring tip, insulated, inner diam. 3 mm, outer diam. 4 mm FDA UDI
- Model / Reference
- GK832R FDA UDI
- Description
- YASARGIL Bipolar Forceps, straight, 9 1/4", (235 mm), working length: 4 1/2", (115 mm), bayonet-shaped, ring tip, insulated, inner diam. 3 mm, outer diam. 4 mm FDA UDI
Identifiers
- Catalog Number
- GK832R FDA UDI
- Primary DI / UDI-DI
- 04038653173891 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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 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 |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI 6d810751-1563-40b0-9019-0fd6de363fb6 36 fields · synced Jun 1, 2026