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Bellinger

FDA UDI

Class I (US FDA UDI)

by Bellinger A/S

Identity

Trade Name
Bellinger FDA UDI
Generic Name
Spectacle frame FDA UDI
Device Name
Spectacle frame FDA UDI
Model / Reference
PINTAIL-241 FDA UDI
Description
Spectacle frame FDA UDI

Identifiers

Primary DI / UDI-DI
05712544159285 FDA UDI
FDA Product Code
HQZ FDA UDI
GMDN Term
Spectacle frame FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5842 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

No

FDA UDI

Category: Spectacle frame

Spectacle frames are custom-made eyeglasses that fit perfectly over your prescription lenses. Bellinger's Spectacle frame is a stylish and comfortable option for individuals looking to upgrade their daily routine.

Similar devices

Also classified as Spectacle frame.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bellinger A/S

Sources (1)

  • FDA UDI d507efbf-e16e-4295-8370-d4b6822d3219 33 fields · synced Aug 3, 2026