Skip to content

Restraint strap 6-010-41-B

by Skytron, LLC

Restraint strap 6-010-41-B is a Class I device made by Skytron, LLC, listed in FDA GUDID since 15 Mar 2019 (UDI-DI 10841736113254), 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 Number10841736113254 UDI-DI Date15 Mar 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  • Withdrawn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
Restraint strap
Generic name
Limb/torso/head restraint, reusable
Model / reference
6-010-41-B
Primary DI / UDI-DI
10841736113254
FDA product code
LWG
GMDN term
Limb/torso/head restraint, reusable
Device class
Class I
Regulation number
878.4950
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LWG (Surgical Table Cushion).

Other devices from Skytron, LLC

See all devices from Skytron, LLC →

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)