Eddie Bauer

FDA UDI

Class I (US FDA UDI)

by Charmant U.s.a.

Identity

Trade Name: Eddie Bauer FDA UDI
Generic Name: Tinted non-prescription spectacles FDA UDI
Device Name: EddieBauer Tortoise 50/20 142M Pontius FDA UDI
Model / Reference: 39440P FDA UDI
Description: EddieBauer Tortoise 50/20 142M Pontius FDA UDI

Identifiers

Catalog Number: 39440P50TT FDA UDI
Primary DI / UDI-DI: 00888989264831 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Tinted non-prescription spectacles

Eddie Bauer by Charmant U.s.a. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Charmant U.s.a.

Sources (1)

FDA UDI 2b32d2de-89c7-4530-8853-e1c6e3403469 34 fields · synced May 30, 2026