Identity
- Trade Name
- ELMED FDA UDI
- Generic Name
- Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
- Device Name
- 5MM DIA., 26 CM, FENESTRATED GRASPER 22 MM, STRAIGHT SERRATED JAWS W/ LONG FENESTRATION FOR ATRAUMATIC GRIP, SINGLE-ACTION, INSULATED SHAFT & HANDLE W/ RF-POST, ROTATABLE-ONE PIECE W/ FLUSHPORT FDA UDI
- Model / Reference
- 52626-41B FDA UDI
- Description
- 5MM DIA., 26 CM, FENESTRATED GRASPER 22 MM, STRAIGHT SERRATED JAWS W/ LONG FENESTRATION FOR ATRAUMATIC GRIP, SINGLE-ACTION, INSULATED SHAFT & HANDLE W/ RF-POST, ROTATABLE-ONE PIECE W/ FLUSHPORT FDA UDI
Identifiers
- Catalog Number
- 52626-41B FDA UDI
- Primary DI / UDI-DI
- 00842180124141 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Rigid endoscopic tissue manipulation forceps, reusable 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
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Rigid endoscopic tissue manipulation forceps, reusable
Elmed by Elmed Incorporated — 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
- Elmed Incorporated
Sources (1)
- FDA UDI 95bb423d-ee73-4aed-9428-b412994dda13 35 fields · synced May 30, 2026