Skip to content

Rescue Ressentials REMZ0001

by Emsrun Group

Rescue Ressentials REMZ0001 is a Class I device made by Emsrun Group, listed in FDA GUDID since 27 Oct 2026 (UDI-DI 06975675785047), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06975675785047 UDI-DI Date27 Oct 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  • Withdrawn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
Rescue Ressentials
Generic name
Cardiopulmonary resuscitation mask, single-use
Model / reference
REMZ0001
Primary DI / UDI-DI
06975675785047
FDA product code
LYU
GMDN term
Cardiopulmonary resuscitation mask, single-use
Device class
Class I
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LYU (Accessory, Surgical Apparel).

Other devices from Emsrun Group

See all devices from Emsrun Group →

Properties

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