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National Hospital Packaging

FDA UDI

Class I (US FDA UDI)

by Surgi-Pak, Inc.

Identity

Trade Name
NATIONAL HOSPITAL PACKAGING FDA UDI
Generic Name
Razor blade FDA UDI
Device Name
PREP BLADE, STAINLESS STEEL, 2.25IN, 2/PKG, STRL FDA UDI
Model / Reference
35-000 FDA UDI
Description
PREP BLADE, STAINLESS STEEL, 2.25IN, 2/PKG, STRL FDA UDI

Identifiers

Catalog Number
35-000 FDA UDI
Primary DI / UDI-DI
00817213021339 FDA UDI
FDA Product Code
LWK FDA UDI
GMDN Term
Razor blade 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

Yes

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

Category: Razor blade

National Hospital Packaging by Surgi-Pak, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Razor blade.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgi-Pak, Inc.

Sources (1)

  • FDA UDI a94fdb0f-6929-4b42-b2f8-ff6f5d17c05c 35 fields · synced May 30, 2026