A portable, hand-held, battery-powered suction device designed to enable an adult to gently suction and clear excessive mucus from the nasal passages of an infant or child to facilitate easier breathing. It consists of a handgrip that contains the batteries, a
| Company | Devices | Share |
|---|---|---|
| Oak Tech Llc | 24 | 21% |
| Shenzhen Kingboom Technology Co., Ltd. | 11 | 10% |
| Dr. Noze Best, Llc | 11 | 10% |
| Clinical Innovations, Llc | 10 | 9% |
| Guangzhou Berrcom Medical Device Co., Ltd | 7 | 6% |
| Dongguan Yiyingmei Technology Co., Ltd. | 6 | 5% |
| Shenzhen Dongjiang Technology Co., Ltd. | 6 | 5% |
| Hetaida Technology Co., Ltd | 6 | 5% |
| Attract Kereskedelmi Es Szolgaltato Korlatolt Felelossegu Tarsasag | 4 | 4% |
| Shenzhen Aoj Health Science & Technology Co., Ltd. | 3 | 3% |
| Shenzhen Lutejiacheng Supply Chain Management Co., Ltd. | 3 | 3% |
| Peno Llc | 3 | 3% |
Company = labeler of record on GUDID. 25 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| BTA | Pump, Portable, Aspiration (Manual Or Powered) | 45 |
| KDQ | Bottle, Collection, Vacuum | 45 |
| KMA | Irrigator, Powered Nasal | 13 |
| BYY | Tube, Aspirating, Flexible, Connecting | 10 |
| JCX | Apparatus, Suction, Ward Use, Portable, Ac-Powered | 4 |
| BSY | Catheters, Suction, Tracheobronchial | 2 |
Use these as the dimensions to specify in a tender line.
112 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Nasal aspirator, electric", from 25 companies. The largest labeler is Oak Tech Llc with 21% of records.
BTA (Pump, Portable, Aspiration (Manual Or Powered)), KDQ (Bottle, Collection, Vacuum), KMA (Irrigator, Powered Nasal), BYY (Tube, Aspirating, Flexible, Connecting)
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.