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Theriome RS24001

by Rda Spot, Uab

Theriome RS24001 is a Class II device made by Rda Spot, Uab, listed in FDA GUDID since 26 Apr 2024 (UDI-DI 04779054720665), 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 Number04779054720665 UDI-DI Date26 Apr 2024ListedStatusListed 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  • Withdrawn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
Theriome
Generic name
Capillary blood collection kit IVD
Model / reference
RS24001
Primary DI / UDI-DI
04779054720665
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
MRI safety
MR Unsafe

Related devices

Category: Capillary blood collection kit IVD

Other devices from Rda Spot, Uab

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Properties

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