Blinq 1

by Rebiscan, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00864816000421 UDI-DI	Date31 Jul 2018Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Blinq
Generic Name: Paediatric strabismus screening scanner
Model / Reference: 1

Primary DI / UDI-DI: 00864816000421
FDA Product Code: PMW
GMDN Term: Paediatric strabismus screening scanner

Device Class: Class II
Regulation Number: 886.1342
GUDID distribution status: In Commercial Distribution

Other devices from Rebiscan, Inc.

Pediatric Vision Scanner

Class II

Properties

Prescription Use
Serial Number

Other properties (12)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Lot / Batch Number: No
Expiration Date: No
Manufacturing Date: No