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Viscoat

FDA UDI

Class III (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
VISCOAT FDA UDI
Generic Name
Aqueous/vitreous humour replacement medium kit FDA UDI
Device Name
VISCOAT 0.50ML 27G<USA FDA UDI
Model / Reference
8065183905 FDA UDI
Description
VISCOAT 0.50ML 27G<USA FDA UDI

Identifiers

Primary DI / UDI-DI
00380651839052 FDA UDI
FDA Product Code
LZP FDA UDI
GMDN Term
Aqueous/vitreous humour replacement medium kit FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.4275 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 0.50 Milliliter FDA UDI

Category: Aqueous/vitreous humour replacement medium kit

Viscoat by Alcon Laboratories, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aqueous/vitreous humour replacement medium kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alcon Laboratories, Inc.

Sources (1)

  • FDA UDI 9f018354-d86b-4d8b-b883-e8e46a6b22cb 35 fields · synced May 30, 2026