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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
Lacrimal procedural cannula FDA UDI
Device Name
Punctal Dilator and Probe [Khan] .70mm x 45mm (22G x 1 3/4in) FDA UDI
Model / Reference
585124 FDA UDI
Description
Punctal Dilator and Probe [Khan] .70mm x 45mm (22G x 1 3/4in) FDA UDI

Identifiers

Primary DI / UDI-DI
30886158101834 FDA UDI
FDA Product Code
HNL FDA UDI
GMDN Term
Lacrimal procedural cannula 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Lacrimal procedural cannula

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

Similar devices

Also classified as Lacrimal procedural cannula.

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 3e9377fa-d96a-4bcb-974b-23e10a752e08 34 fields · synced Jun 8, 2026