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Beaver Visitec Inter

FDA UDI

Class II (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Beaver Visitec Inter FDA UDI
Generic Name
Ophthalmic sponge FDA UDI
Device Name
Eye Fluid Wick 0.40*15cm(5/32*5 7/8in)_non-sterile_3600EA/CS FDA UDI
Model / Reference
581168 FDA UDI
Description
Eye Fluid Wick 0.40*15cm(5/32*5 7/8in)_non-sterile_3600EA/CS FDA UDI

Identifiers

Primary DI / UDI-DI
16931918190563 FDA UDI
FDA Product Code
HOZ FDA UDI
GMDN Term
Ophthalmic sponge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4790 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic sponge

Beaver Visitec Inter by GRI Medical & Electronic Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic sponge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
GRI Medical & Electronic Technology Co., Ltd.

Sources (1)

  • FDA UDI 7f35cc64-8a34-43da-b711-3a123cd8a3e3 34 fields · synced Sep 18, 2026