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Visitec®

FDA UDI

Class I (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name
Visitec® FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
Lacrimal Trephine [Sisler] .80mm x 38mm (21G x 1 1/2in 3 FDA UDI
Model / Reference
585031 FDA UDI
Description
Lacrimal Trephine [Sisler] .80mm x 38mm (21G x 1 1/2in 3 FDA UDI

Identifiers

Catalog Number
585031 FDA UDI
Primary DI / UDI-DI
30886158101339 FDA UDI
FDA Product Code
HRH FDA UDI
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use 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

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: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

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

Similar devices

Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5be8e942-fa28-4875-b1ed-af90a977057b 35 fields · synced Jun 1, 2026