Consulting Wallah › Device Explorer › Syringes, needles & infusion › Pellet implantation cannula, single-use
Device Explorer · FDA GUDID · GMDN 63148

Pellet implantation cannula, single-use

A rigid tube intended for subcutaneous delivery of an implantable drug pellet. The cannula is typically designed with a proximal well/side-hole for pellet loading, and typically includes a trocar blade to assist cannula introduction and a push rod to drive the

US‑registered devices52in commercial distribution
Companies6labelers on GUDID
Single‑use87%of device records
Sterile52%labelled sterile
Prescription8%Rx‑only share
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Share of device records

B. Ali Impex2344%
Apollo Medical Products Corp.2242%
Stradis Medical Llc36%
Br Surgical, Llc24%
Sfm Medical Devices Gmbh12%
Endo Pharmaceuticals Inc.12%

Top labelers

CompanyDevicesShare
B. Ali Impex2344%
Apollo Medical Products Corp.2242%
Stradis Medical Llc36%
Br Surgical, Llc24%
Sfm Medical Devices Gmbh12%
Endo Pharmaceuticals Inc.12%

Company = labeler of record on GUDID. 6 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Cannula for subcutaneous Implant/ pellet adminisBR Surgical, LLCSterling Medical ProductsN/AStradis Medical, LLCDoctor Nice

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

FDA product codes

CodeNameDevices
FBQTrocar, Gastro-Urology23
GEACannula, Surgical, General & Plastic Surgery3
DRCTrocar3
MDMInstrument, Manual, Surgical, General Use1

GMDN & GCC registration

  • GMDN code 63148 · non‑implantable
  • Single‑use 87% · sterile 52% · Rx‑only 8% · OTC 44%
  • 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.

No closely related category with 50+ devices.

How many pellet implantation cannula, single-use products are registered in the US?

52 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Pellet implantation cannula, single-use", from 6 companies. The largest labeler is B. Ali Impex with 44% of records.

Which FDA product codes apply?

FBQ (Trocar, Gastro-Urology), GEA (Cannula, Surgical, General & Plastic Surgery), DRC (Trocar), MDM (Instrument, Manual, Surgical, General Use)

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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