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V. Mueller

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Device operating status label/tag, single-use FDA UDI
Device Name
V. Mueller TAMPER EVIDENT ARROW DBL-BARB STEAM WHT FDA UDI
Model / Reference
AS2-3 FDA UDI
Description
V. Mueller TAMPER EVIDENT ARROW DBL-BARB STEAM WHT FDA UDI

Identifiers

Catalog Number
AS23 FDA UDI
Primary DI / UDI-DI
20885403206464 FDA UDI
510(k) Number
K142529 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Device operating status label/tag, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Category: Device operating status label/tag, single-use

V. Mueller by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device operating status label/tag, single-use.

Cleared under the same submission

K142529 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI d2f607eb-9847-4423-8dfb-dbeb67cfe99b 36 fields · synced Jun 8, 2026