Consulting Wallah › Device Explorer › Other devices › Laminar airflow hood
Device Explorer · FDA GUDID · GMDN 40522

Laminar airflow hood

A ventilated laboratory enclosure designed to prevent airborne biological contamination of laboratory specimens contained within, and personnel handling the specimen, by creating a barrier with a forced flow of uniform-velocity and parallel-direction air. It i

US‑registered devices73in commercial distribution
Companies2labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription18%Rx‑only share
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Share of device records

Coopersurgical, Inc.6082%
Esco Medical Technologies Uab1318%

Top labelers

CompanyDevicesShare
Coopersurgical, Inc.6082%
Esco Medical Technologies Uab1318%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Multi-zone ART WorkstationK-Systems

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

FDA product codes

CodeNameDevices
PUBAccessory, Assisted Reproduction, Exempt73

GMDN & GCC registration

  • GMDN code 40522 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 18% · OTC 0%
  • 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 laminar airflow hood products are registered in the US?

73 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Laminar airflow hood", from 2 companies. The largest labeler is Coopersurgical, Inc. with 82% of records.

Which FDA product codes apply?

PUB (Accessory, Assisted Reproduction, Exempt)

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.

How do I get quotes?

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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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