Consulting Wallah › Device Explorer › Other devices › Non-respiratory device ambient air filter
Device Explorer · FDA GUDID · GMDN 11711

Non-respiratory device ambient air filter

A filter designed to be installed in a non-respiratory device to clean the ambient air that passes through it to facilitate device operation/management. It is composed of tightly woven materials which remove particulates/impurities and, depending on how the de

US‑registered devices99in commercial distribution
Companies10labelers on GUDID
Single‑use22%of device records
Sterile0%labelled sterile
Prescription62%Rx‑only share
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Share of device records

Lifeglobal Group, Llc3535%
Coopersurgical, Inc.2525%
Pentair Filtration Solutions, Llc1919%
Drive Devilbiss Healthcare88%
Black & Black Surgical, Inc.44%
Lifeaire Systems, Llc22%
Icu Medical, Inc.22%
Medline Industries, Inc.22%

Top labelers

CompanyDevicesShare
Lifeglobal Group, Llc3535%
Coopersurgical, Inc.2525%
Pentair Filtration Solutions, Llc1919%
Drive Devilbiss Healthcare88%
Black & Black Surgical, Inc.44%
Lifeaire Systems, Llc22%
Icu Medical, Inc.22%
Medline Industries, Inc.22%
Aesculap Ag11%
Airon Corporation11%

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

Brand names on the register (sample)

AESCULAPLifeGlobal™Aire~LifelinepNeutonN/ACoda®CarexPentairPENTAIRLevel 1Medline

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

FDA product codes

CodeNameDevices
MQGACCESSORY, ASSISTED REPRODUCTION42
CAHFilter, Bacterial, Breathing-Circuit28
MQGAccessory, Assisted Reproduction25
GEACANNULA, SURGICAL, GENERAL & PLASTIC SURGERY4
PUBAccessory, Assisted Reproduction, Exempt2
FMFSyringe, piston2

GMDN & GCC registration

  • GMDN code 11711 · non‑implantable
  • Single‑use 22% · sterile 0% · Rx‑only 62% · OTC 11%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Weight (Pound) · 1Height (Inch) · 1Width (Inch) · 1Length (Inch) · 1

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

No closely related category with 50+ devices.

How many non-respiratory device ambient air filter products are registered in the US?

99 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Non-respiratory device ambient air filter", from 10 companies. The largest labeler is Lifeglobal Group, Llc with 35% of records.

Which FDA product codes apply?

MQG (ACCESSORY, ASSISTED REPRODUCTION), CAH (Filter, Bacterial, Breathing-Circuit), MQG (Accessory, Assisted Reproduction), GEA (CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY)

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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