Device Explorer · FDA GUDID · GMDN 13217

Bedside syringe pump

A mains electricity (AC-powered) non-ambulatory device designed to precisely drive the plunger of a syringe down its barrel to infuse a solution when it must be administered with a high degree of volume accuracy and rate consistency. Because of the lower flow

US‑registered devices51in commercial distribution
Companies9labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription90%Rx‑only share
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Share of device records

Icu Medical, Inc.1835%
B. Braun Medical Inc.1325%
Carefusion 303, Inc.1020%
Baxter Healthcare Corporation48%
Atlanta Biomedical Corporation24%
Spectrum Medical Limited12%
Fresenius Kabi Ag12%
American Iv Products, Inc.12%

Top labelers

CompanyDevicesShare
Icu Medical, Inc.1835%
B. Braun Medical Inc.1325%
Carefusion 303, Inc.1020%
Baxter Healthcare Corporation48%
Atlanta Biomedical Corporation24%
Spectrum Medical Limited12%
Fresenius Kabi Ag12%
American Iv Products, Inc.12%
Cardinal Health 200, Llc12%

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

Brand names on the register (sample)

Novum IQQuantumAGILIA SP MC WIFI USInfusomat®Perfusor®NAAtlanta BioMedical Model 4100AIVMedfusionMEDFUSIONBD Alaris™ Syringe Module Model 8110Alaris™ PCA Module Model 8120Alaris™ PCA Module, Model 8120BD Alaris™ Syringe Module, Model 8110BD® Alaris™ Syringe Module, Model 8110Kangaroo

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

FDA product codes

CodeNameDevices
FRNPump, infusion47
MRZACCESSORIES, PUMP, INFUSION15
FRNPump, Infusion14
MEAPump, infusion, pca14
MEAPump, Infusion, Pca11
LZHPump, infusion, enteral9

GMDN & GCC registration

  • GMDN code 13217 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 90% · OTC 2%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Width (Inch) · 1Length (Inch) · 1

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

How many bedside syringe pump products are registered in the US?

51 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bedside syringe pump", from 9 companies. The largest labeler is Icu Medical, Inc. with 35% of records.

Which FDA product codes apply?

FRN (Pump, infusion), MRZ (ACCESSORIES, PUMP, INFUSION), FRN (Pump, Infusion), MEA (Pump, infusion, pca)

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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