Consulting Wallah › Device Explorer › Procedure kits & trays › Cardiopulmonary resuscitation kit, single-use
Device Explorer · FDA GUDID · GMDN 35693

Cardiopulmonary resuscitation kit, single-use

A collection of items in a portable case intended for cardiopulmonary resuscitation (e.g., airway tubes, face masks, resuscitator). It is typically placed in a convenient location in public buildings and in emergency medical services (EMS) vehicles for quick a

US‑registered devices150in commercial distribution
Companies10labelers on GUDID
Single‑use81%of device records
Sterile0%labelled sterile
Prescription80%Rx‑only share
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Share of device records

Ambu A/S5335%
Xiamen Compower Medical Tech. Co., Ltd5033%
Airlife3423%
Microtek Medical Llc43%
Zoll Medical Corporation21%
Bound Tree Medical, Llc21%
Redicare Llc21%
Philips Electronics North America Corporation11%

Top labelers

CompanyDevicesShare
Ambu A/S5335%
Xiamen Compower Medical Tech. Co., Ltd5033%
Airlife3423%
Microtek Medical Llc43%
Zoll Medical Corporation21%
Bound Tree Medical, Llc21%
Redicare Llc21%
Philips Electronics North America Corporation11%
Physio-Control, Inc.11%
Maybeam Llc11%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CompowerWNL ProductsMFASCOODRESCUEWNLProductsFIRST AID ONLYInkwell Global MarketingEMIWNL ProductWNLAmerican Red CrossWNL productEver Ready First AidAquatic SolutionsDixie EMS Supplycompower

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
OEVCardiopulmonary resuscitation aid kit53
OEVCardiopulmonary Resuscitation Aid Kit41
OKIEmergency response safety kit40
OKIEmergency Response Safety Kit34
CBPValve, non-rebreathing6
CBPValve, Non-Rebreathing4

GMDN & GCC registration

  • GMDN code 35693 · non‑implantable
  • Single‑use 81% · sterile 0% · Rx‑only 80% · OTC 16%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many cardiopulmonary resuscitation kit, single-use products are registered in the US?

150 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cardiopulmonary resuscitation kit, single-use", from 10 companies. The largest labeler is Ambu A/S with 35% of records.

Which FDA product codes apply?

OEV (Cardiopulmonary resuscitation aid kit), OEV (Cardiopulmonary Resuscitation Aid Kit), OKI (Emergency response safety kit), OKI (Emergency Response Safety Kit)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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