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Device Explorer · FDA GUDID · GMDN 43344

Tissue culture/microbiology petri dish, single-use

A device formed as a round and shallow-sided dish intended to be used to grow and contain tissue and/or microbial cultures for laboratory procedures; it is not intended for in vitro fertilization (IVF). It is designed to fit into a range of laboratory instrume

US‑registered devices121in commercial distribution
Companies12labelers on GUDID
Single‑use99%of device records
Sterile95%labelled sterile
Prescription7%Rx‑only share
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Share of device records

Sarstedt Aktiengesellschaft & Co.Kg5545%
Edge Biologicals, Inc.2722%
Medline Industries, Inc.1714%
Vitromed Gmbh65%
Bioseal54%
Sarstedt, Inc.32%
Dynarex Corporation22%
Fisher Scientific Company L.L.C.22%

Top labelers

CompanyDevicesShare
Sarstedt Aktiengesellschaft & Co.Kg5545%
Edge Biologicals, Inc.2722%
Medline Industries, Inc.1714%
Vitromed Gmbh65%
Bioseal54%
Sarstedt, Inc.32%
Dynarex Corporation22%
Fisher Scientific Company L.L.C.22%
Mdhc Life Technologies (Kunshan) Co., Ltd.11%
Esco Medical Technologies Uab11%
Surgi-Pak, Inc.11%
Apollo Medical Products Corp.11%

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

Brand names on the register (sample)

MDHCDish for MIRI TLV-4WELLDISHV-ICSIDISH-50V-CULTUREDISH-35V-CULTUREDISH-90V-CULTUREDISH-60V-CENTERWELL-60TC plate 96 well, BIOFLOAT™,RInsert, 24 Well, PET 8µm, TLInsert, 24 Well, PET 5µm, TLInsert, 24 Well, PET 3µm, TLInsert, 24 Well, PET 1µm, TPInsert, 24 Well, PET 0.4µm, TPInsert, 24 Well, PET 0.4µm, TLInsert, 12 Well, PET 8µm, TL

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

FDA product codes

CodeNameDevices
KIZDISH, TISSUE CULTURE67
JSICulture Media, Selective And Differential16
LIBDEVICE, GENERAL PURPOSE, MICROBIOLOGY, DIAGNOSTIC13
KIZDish, Tissue Culture6
PUDLabware, Assisted Reproduction, Exempt6
JSGCulture Media, Non-Selective And Non-Differential6

GMDN & GCC registration

  • GMDN code 43344 · non‑implantable
  • Single‑use 99% · sterile 95% · Rx‑only 7% · 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 tissue culture/microbiology petri dish, single-use products are registered in the US?

121 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tissue culture/microbiology petri dish, single-use", from 12 companies. The largest labeler is Sarstedt Aktiengesellschaft & Co.Kg with 45% of records.

Which FDA product codes apply?

KIZ (DISH, TISSUE CULTURE), JSI (Culture Media, Selective And Differential), LIB (DEVICE, GENERAL PURPOSE, MICROBIOLOGY, DIAGNOSTIC), KIZ (Dish, Tissue Culture)

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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