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AMSafe® Prep Razor

FDA UDI

Class I (US FDA UDI)

by Amsino International, Inc.

Identity

Trade Name
AMSafe® Prep Razor FDA UDI
Generic Name
Safety razor, single-use FDA UDI
Device Name
AMSafe® Prep Razor FDA UDI
Model / Reference
1 FDA UDI
Description
AMSafe® Prep Razor FDA UDI

Identifiers

Catalog Number
RZPTU01 FDA UDI
Primary DI / UDI-DI
10704411008071 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Safety razor, single-use

AMSafe® Prep Razor by Amsino International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Safety razor, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 08731935-e148-4f27-af74-5fc9234cc7cc 34 fields · synced May 30, 2026