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Bellinger ACEELLIPSE-2-4896

by Bellinger A/S United States GUDID

Product code HQZ

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05712544173533 UDI-DIDate11 Feb 2026ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

GUDID · synced 22 Oct 2026

Trade Name
Bellinger
Generic Name
Spectacle frame
Model / Reference
ACEELLIPSE-2-4896
Primary DI / UDI-DI
05712544173533
FDA Product Code
HQZ
GMDN Term
Spectacle frame
Device Class
Class I
Regulation Number
886.5842
Commercial Distribution
In Commercial Distribution

Other devices from Bellinger A/S

See all devices from Bellinger A/S →

Properties & raw data

Show properties, registry sources and raw records
  • Premarket Exempt
Other properties (13)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI 79a4b426-40c2-440d-a79b-0bb5480d8085 33 fields · synced 22 Oct 2026