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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
Wire/ligature passer, reusable FDA UDI
Device Name
MAYO GOITER LIGATURE CARRIER FULLY CURVED OVERALL LENGTH 8-1/2" (21.6CM) FDA UDI
Model / Reference
SU3985 FDA UDI
Description
MAYO GOITER LIGATURE CARRIER FULLY CURVED OVERALL LENGTH 8-1/2" (21.6CM) FDA UDI

Identifiers

Catalog Number
SU3985 FDA UDI
Primary DI / UDI-DI
10885403133251 FDA UDI
FDA Product Code
GEJ FDA UDI
GMDN Term
Wire/ligature passer, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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 8d054e72-b2ae-46da-953f-7672525962b1 36 fields · synced Sep 18, 2026