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Device Explorer · FDA GUDID · GMDN 64573

Peripheral intravenous catheterization kit, non-sensing

A collection of non-powered devices intended for the introduction of an included peripheral vein cannula, often referred to as a catheter, to enable short-term (= 30 days) intravenous (IV) access for administration of fluids/medication and blood sampling. In a

US‑registered devices78in commercial distribution
Companies8labelers on GUDID
Single‑use100%of device records
Sterile82%labelled sterile
Prescription95%Rx‑only share
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Share of device records

Teleflex Incorporated3140%
Neo Medical Inc.2937%
Bound Tree Medical, Llc810%
North American Rescue, Llc56%
Cardinal Health 200, Llc23%
Nar Medical Depot, Llc11%
Cardinal Health, Inc.11%
Amsino International, Inc.11%

Top labelers

CompanyDevicesShare
Teleflex Incorporated3140%
Neo Medical Inc.2937%
Bound Tree Medical, Llc810%
North American Rescue, Llc56%
Cardinal Health 200, Llc23%
Nar Medical Depot, Llc11%
Cardinal Health, Inc.11%
Amsino International, Inc.11%

Company = labeler of record on GUDID. 8 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

IV Start KitNARNAR KitCuraplexV-CathNeoMagicPowerStickARROWMonojectAMSure® IV Start KitCARDINAL HEALTH

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

FDA product codes

CodeNameDevices
PNDMidline catheter17
FOZCatheter,Intravascular,Therapeutic,Short-Term Less Than 30 D16
LRSI.V. start kit9
LJSCatheter, intravascular, therapeutic, long-term greater than9
LJSCatheter,Intravascular,Therapeutic,Long-Term Greater Than 308
LRSI.V. Start Kit7

GMDN & GCC registration

  • GMDN code 64573 · non‑implantable
  • Single‑use 100% · sterile 82% · Rx‑only 95% · 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

Catheter Gauge (French) · 33Length (Centimeter) · 27Pressure (Pound per Square Inch) · 8Needle Gauge (Gauge) · 4Catheter Length (Centimeter) · 4

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

How many peripheral intravenous catheterization kit, non-sensing products are registered in the US?

78 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Peripheral intravenous catheterization kit, non-sensing", from 8 companies. The largest labeler is Teleflex Incorporated with 40% of records.

Which FDA product codes apply?

PND (Midline catheter), FOZ (Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 D), LRS (I.V. start kit), LJS (Catheter, intravascular, therapeutic, long-term greater than)

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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