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Sea Striker

FDA UDI

Class I (US FDA UDI)

by Cliff Weil, Inc.

Identity

Trade Name
Sea Striker FDA UDI
Generic Name
Tinted non-prescription spectacles FDA UDI
Device Name
SEA STRIKER 270 POLARIZED SUNGLASSES FDA UDI
Model / Reference
270 FDA UDI
Description
SEA STRIKER 270 POLARIZED SUNGLASSES FDA UDI

Identifiers

Catalog Number
270 FDA UDI
Primary DI / UDI-DI
00083758612701 FDA UDI
FDA Product Code
HQY FDA UDI
GMDN Term
Tinted non-prescription spectacles 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tinted non-prescription spectacles

A comprehensive guide to the Sea Striker 270 Polarized Sunglasses, featuring its regulatory compliance, key features, and FAQ answers.

Similar devices

Also classified as Tinted non-prescription spectacles.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cliff Weil, Inc.

Sources (1)

  • FDA UDI 1c9aedf7-57de-4500-8fd4-e8ef646426bf 34 fields · synced Jul 2, 2026