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Broselow™ 7700YIN

by Airlife, Inc.

Broselow™ 7700YIN is a Class II device made by Airlife, Inc., listed in FDA GUDID since 14 Feb 2025 (UDI-DI 10889483589069), 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 Number10889483589069 UDI-DI Date14 Feb 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  • Withdrawn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
Broselow™
Generic name
Cardiopulmonary resuscitation kit, single-use
Model / Ref / Catalog
7700YIN
Primary DI / UDI-DI
10889483589069
FDA product code
OKI
GMDN term
Cardiopulmonary resuscitation kit, single-use
Device class
Class II
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiopulmonary resuscitation kit, single-use

Other devices from Airlife, Inc.

See all devices from Airlife, Inc. →

Properties

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