← Back to catalogue

V. Mueller

FDA UDI

Class II (US FDA UDI)

by Carefusion 2200, Inc.

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Device Name
V. Mueller BULLET W/SPOON GRASPER 5MM, 45CM INSERT FDA UDI
Model / Reference
256.79020B FDA UDI
Description
V. Mueller BULLET W/SPOON GRASPER 5MM, 45CM INSERT FDA UDI

Identifiers

Catalog Number
256.79020B FDA UDI
Primary DI / UDI-DI
10885403135309 FDA UDI
510(k) Number
K974382 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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
Sterilization Method
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

K974382 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Carefusion 2200, Inc.

Sources (1)

  • FDA UDI 27cb9618-e02d-47fd-a74c-f12b9e2ebcef 37 fields · synced Sep 18, 2026