Skip to content

Forcecord MCRD5580

by Xiros Ltd

Forcecord MCRD5580 is a Class I device made by Xiros Ltd, listed in FDA GUDID since 6 Jul 2026 (UDI-DI 05060267134547), 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 Number05060267134547 UDI-DI Date6 Jul 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  • Withdrawn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
Forcecord
Generic name
Surgical support tape, non-bioabsorbable
Model / reference
MCRD5580
Primary DI / UDI-DI
05060267134547
FDA product code
OJH
GMDN term
Surgical support tape, non-bioabsorbable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Similar devices

Other devices filed under FDA product code OJH (Orthopedic Tray).

Other devices from Xiros Ltd

See all devices from Xiros Ltd →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)