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Podiatry

FDA UDI

Class I (US FDA UDI)

by Timesco Healthcare Limited

Identity

Trade Name
Podiatry FDA UDI
Generic Name
Nail clippers, reusable FDA UDI
Device Name
Thwaite Nail Cutter 5.5" Fine Blade FDA UDI
Model / Reference
10.352.50 FDA UDI
Description
Thwaite Nail Cutter 5.5" Fine Blade FDA UDI

Identifiers

Catalog Number
10.352.50 FDA UDI
Primary DI / UDI-DI
05055382802679 FDA UDI
FDA Product Code
FZT 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Nail clippers, reusable

Podiatry by Timesco Healthcare Limited — 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
Timesco Healthcare Limited

Sources (1)

  • FDA UDI 5e3ccda4-578a-4a4d-a30d-632e6b4bca32 35 fields · synced May 30, 2026