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Beaver®

FDA UDI

Class I (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name
Beaver® FDA UDI
Generic Name
Meniscus knife FDA UDI
Device Name
BLADE 4.0MM POINTED TIP CURVED LEFT S/SU (6/SP) FDA UDI
Model / Reference
376780 FDA UDI
Description
BLADE 4.0MM POINTED TIP CURVED LEFT S/SU (6/SP) FDA UDI

Identifiers

Catalog Number
376780 FDA UDI
Primary DI / UDI-DI
30886158001240 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Meniscus knife 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Meniscus knife

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

Similar devices

Also classified as Meniscus knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beaver-Visitec International, Inc.

Sources (1)

  • FDA UDI e860176b-37a3-46f3-9ec4-f15109453e8e 36 fields · synced May 31, 2026