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Nano-Check™ Influenza A+B Test MD8153

by Nano-Ditech Corporation GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00895160002878 UDI-DIDate22 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Nano-Check™ Influenza A+B Test
Generic Name
Influenza A/B virus antigen IVD, kit, rapid ICT, clinical
Model / Reference
MD8153
Primary DI / UDI-DI
00895160002878
GMDN Term
Influenza A/B virus antigen IVD, kit, rapid ICT, clinical
GUDID distribution status
In Commercial Distribution

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See all devices from Nano-Ditech Corporation →

Properties

  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No