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Device Explorer · FDA GUDID · GMDN 16631

Non-absorbing intravenous administration set

A collection of sterile devices designed for the intravenous (IV) administration of solutions and manufactured with low-absorption plastics to avoid partial absorption of the components of the infused solutions. It typically consists of plastic tubes made of o

US‑registered devices60in commercial distribution
Companies3labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription98%Rx‑only share
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Share of device records

Centurion Medical Products Corporation5592%
Medical Technology Products Inc47%
Codan Us Corporation12%

Top labelers

CompanyDevicesShare
Centurion Medical Products Corporation5592%
Medical Technology Products Inc47%
Codan Us Corporation12%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CenturionMTPCodan

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

FDA product codes

CodeNameDevices
FPASet, administration, intravascular58
FPASet, Administration, Intravascular1
FOZCatheter,intravascular,therapeutic,short-term less than 30 d1

GMDN & GCC registration

  • GMDN code 16631 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 98% · 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 non-absorbing intravenous administration set products are registered in the US?

60 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Non-absorbing intravenous administration set", from 3 companies. The largest labeler is Centurion Medical Products Corporation with 92% of records.

Which FDA product codes apply?

FPA (Set, administration, intravascular), FPA (Set, Administration, Intravascular), FOZ (Catheter,intravascular,therapeutic,short-term less than 30 d)

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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