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Sherlock 9770352R

by Bard Access Systems, Inc.

Sherlock 9770352R is a Class II device made by Bard Access Systems, Inc., listed in FDA GUDID since 28 Aug 2019 (UDI-DI 00801741175459), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741175459 UDI-DI Date28 Aug 2019ListedStatusListed 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  • Withdrawn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
Sherlock
Generic name
Patient positioning sensor
Model / Ref / Catalog
9770352R
Primary DI / UDI-DI
00801741175459
FDA product code
LJS
GMDN term
Patient positioning sensor
Device class
Class II
Regulation number
880.5970
GUDID distribution status
In Commercial Distribution

Related devices

Category: Patient positioning sensor

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Other devices filed under Patient positioning sensor.

Other devices from Bard Access Systems, Inc.

See all devices from Bard Access Systems, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)