Consulting Wallah › Device Explorer › Other devices › Intravenous line filter
Device Explorer · FDA GUDID · GMDN 35072

Intravenous line filter

A sterile device designed to remove microorganisms and particulate matter from solutions in an infusion/intravenous (IV) line; it can also be used to remove air. This is a single-use device.

US‑registered devices68in commercial distribution
Companies12labelers on GUDID
Single‑use99%of device records
Sterile79%labelled sterile
Prescription72%Rx‑only share
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Share of device records

Vygon Corporation1421%
Global Life Sciences Solutions Usa Llc1421%
Baxter Healthcare Corporation1218%
Icu Medical, Inc.913%
Baxter International Inc.710%
Codan Us Corporation46%
Pall International Sàrl23%
Asset Medikal Tasarim Sanayi Ve Ticaret Anonim Sirketi23%

Top labelers

CompanyDevicesShare
Vygon Corporation1421%
Global Life Sciences Solutions Usa Llc1421%
Baxter Healthcare Corporation1218%
Icu Medical, Inc.913%
Baxter International Inc.710%
Codan Us Corporation46%
Pall International Sàrl23%
Asset Medikal Tasarim Sanayi Ve Ticaret Anonim Sirketi23%
Gambro Industries11%
Merck Millipore Limited11%
B. Braun Medical Inc.11%
Mps Medical, Inc11%

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

Brand names on the register (sample)

DIACLEARPall Supor® AEF FilterCathivex-GVFilterflow®VYGONSet, I.V. Fluid TransferPall Supor® 5.0 FilterPall Supor® 1.2 FilterPall Posidyne® ELD FilterPall Posidyne® NEO FilterPall® Total Nutrient Admixture FilterCLEARLINK/DUO-VENTCLEARLINKINTERLINKCLEARLINK/CONTINU-FLOEXTENSION SET

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

FDA product codes

CodeNameDevices
FPBFilter, infusion line34
FPASet, administration, intravascular19
FPASet, Administration, Intravascular6
FPBFilter, Infusion Line5
BSPNEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)2
KZLDEVICE, WARMING. BLOOD AND PLASMA2

GMDN & GCC registration

  • GMDN code 35072 · non‑implantable
  • Single‑use 99% · sterile 79% · Rx‑only 72% · 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

Pore Size (Micrometer) · 16

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

How many intravenous line filter products are registered in the US?

68 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intravenous line filter", from 12 companies. The largest labeler is Vygon Corporation with 21% of records.

Which FDA product codes apply?

FPB (Filter, infusion line), FPA (Set, administration, intravascular), FPA (Set, Administration, Intravascular), FPB (Filter, Infusion Line)

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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