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V. Mueller

FDA UDI

Class I (US FDA UDI)

by Carefusion 2200, Inc.

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Open-surgery ligation clip applier FDA UDI
Device Name
V. Mueller SWEET CLIP APPLYING FORCEPS FOR MCKENZIE CLIPS ANGLED SHANKS, STRAIGHT JAWS OVERALL LENGTH 9-1/4" (23.5CM) FDA UDI
Model / Reference
CH2640 FDA UDI
Description
V. Mueller SWEET CLIP APPLYING FORCEPS FOR MCKENZIE CLIPS ANGLED SHANKS, STRAIGHT JAWS OVERALL LENGTH 9-1/4" (23.5CM) FDA UDI

Identifiers

Catalog Number
CH2640 FDA UDI
Primary DI / UDI-DI
10885403026430 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Open-surgery ligation clip applier FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

Yes

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 I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1c179c08-d93d-49cb-b000-e67fd785e4ff 36 fields · synced Sep 18, 2026