Neil Medical

FDA UDI

Class I (US FDA UDI)

by Neil Medical Group

Identity

Trade Name: NEIL MEDICAL FDA UDI
Generic Name: Safety razor, single-use FDA UDI
Device Name: Personal Tripple Blade Razor FDA UDI
Model / Reference: Disposable Razor FDA UDI
Description: Personal Tripple Blade Razor FDA UDI

Identifiers

Catalog Number: Disposable Razor FDA UDI
Primary DI / UDI-DI: 00850063139328 FDA UDI
FDA Product Code: LWK FDA UDI
GMDN Term: Safety razor, 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Safety razor, single-use

Neil Medical by Neil Medical Group — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Neil Medical Group

Sources (1)

FDA UDI 3a765ede-8504-4c46-b214-84ed675470ca 34 fields · synced Jun 6, 2026