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Nail Care

FDA UDI

Class I (US FDA UDI)

by Therafin Corporation

Identity

Trade Name
Nail Care FDA UDI
Generic Name
Assistive nail clippers FDA UDI
Device Name
SUCTION BASE NAIL CARE CENTER FDA UDI
Model / Reference
30056 FDA UDI
Description
SUCTION BASE NAIL CARE CENTER FDA UDI

Identifiers

Catalog Number
30056 FDA UDI
Primary DI / UDI-DI
00840252903137 FDA UDI
FDA Product Code
ILW FDA UDI
GMDN Term
Assistive nail clippers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Assistive nail clippers

Nail Care by Therafin Corporation — 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 a32e0d4b-2ecb-4369-b2b0-94c6b80e22bc 35 fields · synced May 30, 2026