Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
- Device Name
- ADTEC SINGLE USE Grasping Forceps, shaft only, (310 mm), diam. 5 mm, pike-mouth, double action, sterile, reposable, to be used with:PM950R, PM951R, PM953R, PM954R, PM957R, PO958R, PO959R, package of 10 pieces FDA UDI
- Model / Reference
- PO892SU FDA UDI
- Description
- ADTEC SINGLE USE Grasping Forceps, shaft only, (310 mm), diam. 5 mm, pike-mouth, double action, sterile, reposable, to be used with:PM950R, PM951R, PM953R, PM954R, PM957R, PO958R, PO959R, package of 10 pieces FDA UDI
Identifiers
- Catalog Number
- PO892SU FDA UDI
- Primary DI / UDI-DI
- 04046963343439 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
A comprehensive, user-friendly medical device directory for the ADTEC SINGLE USE Grasping Forceps (AESCULAP) device.
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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 87805d86-7445-468d-bc4f-7ec469f1b567 36 fields · synced Oct 6, 2026