Pryor 235

by Pryor Products

Pryor 235 is a Class I device made by Pryor Products, listed in FDA GUDID since 1 Jan 2020 (UDI-DI 00761887001251), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00761887001251 UDI-DI	Date1 Jan 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00761887001251

Coverage

1 jurisdiction

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Withdrawn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: 235

Primary DI / UDI-DI: 00761887001251
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

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Properties

Premarket exempt
Lot / batch number
Manufacturing date

Other properties (12, all answered No)