Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
- Device Name
- GRASPER, TENACULUM, 45CM, TA FDA UDI
- Model / Reference
- 88-8534 FDA UDI
- Description
- GRASPER, TENACULUM, 45CM, TA FDA UDI
Identifiers
- Catalog Number
- 88-8534 FDA UDI
- Primary DI / UDI-DI
- 10885403284885 FDA UDI
- 510(k) Number
- K925079 FDA UDI
- FDA Product Code
- HET FDA UDI
- GMDN Term
- Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1720 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 II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K925079 also covers:
- 10mm Babcock Short Jaw, 35cm, Ratcheting Handle, With Rotation — ENCISION, INC.
- 5mm Atraumatic Grasper, Slide Lock Handle — ENCISION, INC.
- 5mm Debakey Tissue Forcep, Ratcheting Handle, With Rotation, 35cm — ENCISION, INC.
- 5mm Endo Babcock Forcep, Ratcheting Handle, With Rotation — ENCISION, INC.
- Curved Maryland Dissector, 23mm Jaw, Ratcheting Handle With Rotation, 45cm — ENCISION, INC.
- Endoplus — Endoplus
- Endoplus — Endoplus
- Endoplus — Endoplus
- Endoplus — Endoplus
- Endoplus — Endoplus
- Endoplus — Endoplus
- Endoplus — Endoplus
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI 767ddea9-15fd-4a05-bebd-28293a1c8b5b 37 fields · synced Sep 18, 2026