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V. Mueller

FDA UDI

Class II (US FDA UDI)

by Carefusion 2200, Inc

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Stopcock FDA UDI
Device Name
V. Mueller STOPCOCK FEMALE TO MALE LUER-LOCK TIP & FEMALE LUER-LOCK RIGHT SIDE CONNECTION FDA UDI
Model / Reference
HY23156 FDA UDI
Description
V. Mueller STOPCOCK FEMALE TO MALE LUER-LOCK TIP & FEMALE LUER-LOCK RIGHT SIDE CONNECTION FDA UDI

Identifiers

Catalog Number
HY23156 FDA UDI
Primary DI / UDI-DI
10885403051852 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Stopcock FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 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 II — 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 8b4c07a4-b636-4842-89a2-fe4aa4a20935 36 fields · synced Jun 8, 2026