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80217

by PENTAX of America Inc.

80217 is a Class I device made by PENTAX of America Inc., listed in FDA GUDID since 1 Mar 2018 (UDI-DI 04961333240975), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04961333240975 UDI-DI Date1 Mar 2018ListedStatusListed 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  • Withdrawn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

Generic name
Transportable medical equipment stand, non-powered
Model / reference
80217
Primary DI / UDI-DI
04961333240975
FDA product code
BZN
GMDN term
Transportable medical equipment stand, non-powered
Device class
Class I
Regulation number
868.6175
GUDID distribution status
In Commercial Distribution

Related devices

Category: Transportable medical equipment stand, non-powered

Similar devices in this category

Other devices filed under Transportable medical equipment stand, non-powered.

Other devices from PENTAX of America Inc.

See all devices from PENTAX of America Inc. →

Properties

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