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Ac Device Insul

by Lockdown Medical Ltd

Ac Device Insul is a device made by Lockdown Medical Ltd, listed in FDA GUDID since 27 Feb 2019 (UDI-DI 05060433600753), 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 Number05060433600753 UDI-DI Date27 Feb 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  • Withdrawn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
Ac Device
Generic name
Ligament reconstruction instrument set, single-use
Model / Ref / Catalog
INSUL
Primary DI / UDI-DI
05060433600753
GMDN term
Ligament reconstruction instrument set, single-use
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ligament reconstruction instrument set, single-use

Other devices from Lockdown Medical Ltd

See all devices from Lockdown Medical Ltd →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)