Skip to content

SkinFix 2703/50

by Ambu A/S

SkinFix 2703/50 is a Class I device made by Ambu A/S, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 05707480024278), 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 Number05707480024278 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
SkinFix
Generic name
Cable/lead/sensor non-conductive skin-adherent patch, single-use
Model / Ref / Catalog
2703/50
Primary DI / UDI-DI
05707480024278
FDA product code
KGX
GMDN term
Cable/lead/sensor non-conductive skin-adherent patch, single-use
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KGX (Tape and bandage, adhesive).

Other devices from Ambu A/S

See all devices from Ambu A/S →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)