Beaver

FDA UDI

Class I (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name: Beaver FDA UDI
Generic Name: Corneal trephine manual instrument FDA UDI
Device Name: TREPHINE BLADE 11.5MM STERILE 1/EA FDA UDI
Model / Reference: 9550013 FDA UDI
Description: TREPHINE BLADE 11.5MM STERILE 1/EA FDA UDI

Identifiers

Catalog Number: 9550013 FDA UDI
Primary DI / UDI-DI: 00886158011385 FDA UDI
FDA Product Code: HRH FDA UDI
GMDN Term: Corneal trephine manual instrument FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Corneal trephine manual instrument

Beaver by Beaver-Visitec International, Inc. — 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: Beaver-Visitec International, Inc.

Sources (1)

FDA UDI c661d707-cecd-4934-a894-aa5c979b4017 34 fields · synced Jun 8, 2026