An electrically-powered device, which may include noninvasive accessories, intended to generate negative pressure for aspiration of body cavities/wounds during a variety of surgical procedures (e.g., general surgery, liposuction, and laparoscopy), typically to
| Company | Devices | Share |
|---|---|---|
| Medela Ag | 20 | 37% |
| Keymed (Medical & Industrial Equipment) Limited | 12 | 22% |
| Rocket Medical Plc | 4 | 7% |
| The Wells Johnson Company | 4 | 7% |
| Ardo Medical Ag | 3 | 6% |
| Nouvag Ag | 3 | 6% |
| Taiwan Biomaterial Company Limited | 2 | 4% |
| Gi Supply, Inc. | 2 | 4% |
| Shenzhen Hugemed Medical Technical Development Co., Ltd. | 1 | 2% |
| Atmos Medizintechnik Gmbh & Co. Kg | 1 | 2% |
| Livanova Deutschland Gmbh | 1 | 2% |
| Black & Black Surgical, Inc. | 1 | 2% |
Company = labeler of record on GUDID. 12 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) | 36 |
| FEM | Accessories, Photographic, For Endoscope (Exclude Light Sour | 12 |
| MUU | System, Suction, Lipoplasty | 10 |
| QPB | System, Suction, Lipoplasty For Removal | 9 |
| GCX | Apparatus, Suction, Operating-Room, Wall Vacuum Powered | 8 |
| HDB | Extractor, Vacuum, Fetal | 6 |
Use these as the dimensions to specify in a tender line.
54 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical suction pump", from 12 companies. The largest labeler is Medela Ag with 37% of records.
BTA (Pump, Portable, Aspiration (Manual Or Powered)), FEM (Accessories, Photographic, For Endoscope (Exclude Light Sour), MUU (System, Suction, Lipoplasty), QPB (System, Suction, Lipoplasty For Removal)
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.