An assembly of vacuum-powered devices, which includes a surgically invasive component, designed to aspirate unwanted materials (e.g., debris, tissues, fluids) from body cavities/wounds during a surgical procedure (e.g., general surgery, laparoscopy); it may in
| Company | Devices | Share |
|---|---|---|
| Allied Medical, Llc | 75 | 38% |
| Medline Industries, Inc. | 35 | 18% |
| Novosci Corp. | 24 | 12% |
| Cardinal Health 200, Llc | 11 | 6% |
| Scanlan International Inc | 11 | 6% |
| Wuxi Emsrun Technology Co., Ltd. | 9 | 5% |
| Rebound Therapeutics Corporation | 6 | 3% |
| Tianjin Newtrans Technology Development | 5 | 3% |
| Innovative Med | 5 | 3% |
| Smith & Nephew, Inc. | 4 | 2% |
| Precision Medical, Inc. | 4 | 2% |
| Elliquence, Llc | 3 | 2% |
Company = labeler of record on GUDID. 18 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) | 62 |
| GAZ | TUBING, NONINVASIVE | 28 |
| DTS | Sucker, Cardiotomy Return, Cardiopulmonary Bypass | 23 |
| KDQ | Bottle, Collection, Vacuum | 22 |
| JCX | Apparatus, Suction, Ward Use, Portable, Ac-Powered | 18 |
| BYZ | TRAP, STERILE SPECIMEN | 18 |
Use these as the dimensions to specify in a tender line.
199 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "General-purpose surgical suction system, vacuum", from 18 companies. The largest labeler is Allied Medical, Llc with 38% of records.
BTA (Pump, Portable, Aspiration (Manual Or Powered)), GAZ (TUBING, NONINVASIVE), DTS (Sucker, Cardiotomy Return, Cardiopulmonary Bypass), KDQ (Bottle, Collection, Vacuum)
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.