Skip to content

Pryor RD-01021

by Pryor Products

Pryor RD-01021 is a Class I device made by Pryor Products, listed in FDA GUDID since 1 Oct 2026 (UDI-DI 00761887005532), 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 Number00761887005532 UDI-DI Date1 Oct 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  • Withdrawn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
Pryor
Generic name
Freestanding/bed-attached intravenous pole
Model / Ref / Catalog
RD-01021
Primary DI / UDI-DI
00761887005532
FDA product code
FOX
GMDN term
Freestanding/bed-attached intravenous pole
Device class
Class I
Regulation number
880.6990
GUDID distribution status
In Commercial Distribution

Other devices from Pryor Products

See all devices from Pryor Products →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)