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V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Nail clippers, reusable FDA UDI
Device Name
Affinity CUTICLE NIPPER CONVEX EDGE, SINGLE SPRING OVERALL LENGTH 4-1/3 inches 11CM FDA UDI
Model / Reference
SA15085 FDA UDI
Description
Affinity CUTICLE NIPPER CONVEX EDGE, SINGLE SPRING OVERALL LENGTH 4-1/3 inches 11CM FDA UDI

Identifiers

Catalog Number
SA15085 FDA UDI
Primary DI / UDI-DI
10885403121982 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Nail clippers, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
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

Category: Nail clippers, reusable

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

Similar devices

Also classified as Nail clippers, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI a4583c13-dce3-4729-829c-f2a61d49f978 35 fields · synced Jun 6, 2026