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Lsss RM06008

by Lockdown Medical Ltd

Lsss RM06008 is a Class I device made by Lockdown Medical Ltd, listed in FDA GUDID since 24 Jul 2020 (UDI-DI 05060433600906), 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 Number05060433600906 UDI-DI Date24 Jul 2020ListedStatusListed 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  • Withdrawn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
Lsss
Generic name
Surgical depth gauge, reusable
Model / Ref / Catalog
RM06008
Primary DI / UDI-DI
05060433600906
FDA product code
MDM, HTJ, EIL
GMDN term
Surgical depth gauge, reusable
Device class
Class I
Regulation number
878.4800, 888.4300, 872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical depth gauge, reusable

Similar devices in this category

Other devices filed under Surgical depth gauge, reusable.

Other devices from Lockdown Medical Ltd

See all devices from Lockdown Medical Ltd →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)