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CellSHILED SK-3/2-CL

by Equashield Medical Ltd

CellSHILED SK-3/2-CL is a Class I device made by Equashield Medical Ltd, listed in FDA GUDID since 20 Jul 2025 (UDI-DI 07290020288103), 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 Number07290020288103 UDI-DI Date20 Jul 2025ListedStatusListed 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  • Withdrawn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
CellSHILED
Generic name
Compounding transfer set
Model / reference
SK-3/2-CL
Primary DI / UDI-DI
07290020288103
FDA product code
LXG
GMDN term
Compounding transfer set
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Compounding transfer set

Similar devices

Other devices filed under FDA product code LXG (Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use).

Other devices from Equashield Medical Ltd

See all devices from Equashield Medical Ltd →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)