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SleepSense 8210NW

by S. L. P. Scientific Laboratory Products Ltd

SleepSense 8210NW is a Class II device made by S. L. P. Scientific Laboratory Products Ltd, listed in FDA GUDID since 8 Sep 2026 (UDI-DI 07290016714265), 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 Number07290016714265 UDI-DI Date8 Sep 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  • Withdrawn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
SleepSense
Generic name
Respiratory oxygen sensor
Model / reference
8210NW
Primary DI / UDI-DI
07290016714265
FDA product code
DQA
GMDN term
Respiratory oxygen sensor
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DQA (Oximeter).

Other devices from S. L. P. Scientific Laboratory Products Ltd

See all devices from S. L. P. Scientific Laboratory Products Ltd →

Properties

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