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Nail Splitter

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
NAIL SPLITTER FDA UDI
Generic Name
Nail splitting forceps, single-use FDA UDI
Device Name
NAIL SPLITTER 4 INCH GRIP HANDLE FDA UDI
Model / Reference
NAIL SPLITTER FDA UDI
Description
NAIL SPLITTER 4 INCH GRIP HANDLE FDA UDI

Identifiers

Catalog Number
NS400 FDA UDI
Primary DI / UDI-DI
B974NS4000 FDA UDI
FDA Product Code
KDC FDA UDI
GMDN Term
Nail splitting forceps, single-use 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 4 Inch FDA UDI

Category: Nail splitting forceps, single-use

Nail Splitter by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nail splitting forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dr.frigz International(pvt)ltd,

Sources (1)

  • FDA UDI 0aaf3f94-f0ff-4d06-9dab-95be08a2238e 35 fields · synced May 30, 2026