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Mini-Blade®

FDA UDI

Class I (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name
Mini-Blade® FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Device Name
LAMELLAR BLADE 60 DEGREES BEVEL-UP (3EA) FDA UDI
Model / Reference
BEAVER6600 FDA UDI
Description
LAMELLAR BLADE 60 DEGREES BEVEL-UP (3EA) FDA UDI

Identifiers

Catalog Number
BEAVER6600 FDA UDI
Primary DI / UDI-DI
30886158004432 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Manual scalpel blade, 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manual scalpel blade, single-use

Mini-Blade® by Beaver-Visitec International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual scalpel blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1bc3ebf4-c208-4480-a0fa-b958e2c06608 35 fields · synced Jun 1, 2026