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Nds NDS90R0070

by PENTAX of America Inc.

Nds NDS90R0070 is a Class I device made by PENTAX of America Inc., listed in FDA GUDID since 15 Mar 2018 (UDI-DI 04961333244065), 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 Number04961333244065 UDI-DI Date15 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  • Withdrawn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

Trade name
Nds
Generic name
Endoscopic video image display unit
Model / reference
NDS90R0070
Primary DI / UDI-DI
04961333244065
FDA product code
KQM
GMDN term
Endoscopic video image display unit
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution
Size
Length — 42.0 Inch

Similar devices

Other devices filed under FDA product code KQM (Camera, Surgical And Accessories).

Other devices from PENTAX of America Inc.

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)