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RDA Spot RS26001

by Rda Spot, Uab

RDA Spot RS26001 is a Class II device made by Rda Spot, Uab, listed in FDA GUDID since 15 Jan 2026 (UDI-DI 04779054721198), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04779054721198 UDI-DI Date15 Jan 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
RDA Spot
Generic name
Capillary blood collection kit IVD
Model / reference
RS26001
Primary DI / UDI-DI
04779054721198
FDA product code
PQD
GMDN term
Capillary blood collection kit IVD
Device class
Class II
Regulation number
862.1675
GUDID distribution status
In Commercial Distribution

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)