Consulting Wallah › Device Explorer › Syringes, needles & infusion › Peripheral nerve-block blunt needle/cannula kit
Device Explorer · FDA GUDID · GMDN 59013

Peripheral nerve-block blunt needle/cannula kit

A collection of sterile devices intended to provide percutaneous access to a peripheral nerve group for injection of an anaesthetic/analgesic agent for nerve-block/pain control (e.g., sleeve blocks, deep muscle blocks, hypogastric blocks, paravertebral blocks,

US‑registered devices412in commercial distribution
Companies2labelers on GUDID
Single‑use100%of device records
Sterile98%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Cardinal Health 200, Llc38994%
Aligned Medical Solutions236%

Top labelers

CompanyDevicesShare
Cardinal Health 200, Llc38994%
Aligned Medical Solutions236%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Aligned Medical SolutionsCARDINAL HEALTH

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

FDA product codes

CodeNameDevices
OGJNerve block tray308
OGJNerve block tray (kit)90
OFQAnesthesia kit12
OJGNeurological tray1
OHMCesarean section tray1

GMDN & GCC registration

  • GMDN code 59013 · non‑implantable
  • Single‑use 100% · sterile 98% · Rx‑only 100% · 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 peripheral nerve-block blunt needle/cannula kit products are registered in the US?

412 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Peripheral nerve-block blunt needle/cannula kit", from 2 companies. The largest labeler is Cardinal Health 200, Llc with 94% of records.

Which FDA product codes apply?

OGJ (Nerve block tray), OGJ (Nerve block tray (kit)), OFQ (Anesthesia kit), OJG (Neurological tray)

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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