← Back to catalogue

Berkley

FDA UDI

Class I (US FDA UDI)

by Pure Fishing, Inc.

Identity

Trade Name
Berkley FDA UDI
Generic Name
Tinted non-prescription spectacle lens FDA UDI
Device Name
Sunglasses FDA UDI
Model / Reference
1362233 FDA UDI
Description
Sunglasses FDA UDI

Identifiers

Primary DI / UDI-DI
00028632713297 FDA UDI
FDA Product Code
HQY FDA UDI
GMDN Term
Tinted non-prescription spectacle lens FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tinted non-prescription spectacle lens

Berkley by Pure Fishing, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tinted non-prescription spectacle lens.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Pure Fishing, Inc.

Sources (1)

  • FDA UDI d73079cc-fc10-47b2-83cb-8fb32801a083 34 fields · synced May 31, 2026