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Device Explorer · FDA GUDID · GMDN 45410

User-induced micropipette

A long, thin tube made of glass or plastic typically used in the laboratory for the manual withdrawal, transfer, and injection of minute volumes of fluid materials (e.g., microlitres or smaller). The user will typically attach a mouthpiece and create a partial

US‑registered devices429in commercial distribution
Companies9labelers on GUDID
Single‑use100%of device records
Sterile97%labelled sterile
Prescription88%Rx‑only share
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Share of device records

Vitrolife Inc.16538%
Vitrolife Sweden Ab14233%
Spectrum Fertility Group Inc.4410%
Cook Vandergrift Inc.317%
Donnevie Medical Technology(Shanghai)Co.Ltd215%
Guangzhou Pinzhi Medical Device Co., Ltd.92%
Medline Industries, Inc.72%
Cook Incorporated51%

Top labelers

CompanyDevicesShare
Vitrolife Inc.16538%
Vitrolife Sweden Ab14233%
Spectrum Fertility Group Inc.4410%
Cook Vandergrift Inc.317%
Donnevie Medical Technology(Shanghai)Co.Ltd215%
Guangzhou Pinzhi Medical Device Co., Ltd.92%
Medline Industries, Inc.72%
Cook Incorporated51%
Marketlab Inc.51%

Company = labeler of record on GUDID. 9 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Denudation PipettesBiopsy pipettesCOOKCook FlexipetCookMarketlabHandling PipetteMedlineICSI PipetteHolding PipetteBiopsy PipettePZD PipetteHatching PipetteDEWINHolding pipettesSFG Biopsy pipettes

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

FDA product codes

CodeNameDevices
PUCMicrotools, Assisted Reproduction (Pipettes), Exempt209
MQHMicrotools, Assisted Reproduction (Pipettes)203
MQHMICROTOOLS, ASSISTED REPRODUCTION (PIPETTES)32
GJWPIPETTE, PASTEUR6
LXGEquipment, Laboratory, General Purpose, Labeled Or Promoted 5
PUCMicrotools, assisted reproduction (pipettes), exempt4

GMDN & GCC registration

  • GMDN code 45410 · non‑implantable
  • Single‑use 100% · sterile 97% · Rx‑only 88% · 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 user-induced micropipette products are registered in the US?

429 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "User-induced micropipette", from 9 companies. The largest labeler is Vitrolife Inc. with 38% of records.

Which FDA product codes apply?

PUC (Microtools, Assisted Reproduction (Pipettes), Exempt), MQH (Microtools, Assisted Reproduction (Pipettes)), MQH (MICROTOOLS, ASSISTED REPRODUCTION (PIPETTES)), GJW (PIPETTE, PASTEUR)

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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