Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Rigid endoscopic grasping forceps, reusable FDA UDI
- Device Name
- DIAMOND-TOUCH® GRASPER INSULATED FUNDUS 26CM (10"), 3,5MM SHAFT FDA UDI
- Model / Reference
- 89-2372 FDA UDI
- Description
- DIAMOND-TOUCH® GRASPER INSULATED FUNDUS 26CM (10"), 3,5MM SHAFT FDA UDI
Identifiers
- Catalog Number
- 89-2372 FDA UDI
- Primary DI / UDI-DI
- 10885403156014 FDA UDI
- 510(k) Number
- K960400 FDA UDI
- FDA Product Code
- FBM FDA UDI
- GMDN Term
- Rigid endoscopic grasping forceps, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5090 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
V. Mueller by Carefusion 2200, 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
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI 4b9f493c-d9b0-4d48-a1b4-18f2d378695e 37 fields · synced Sep 18, 2026