A device intended to be connected between a thoracic drainage catheter (not included) and a suction wall outlet, to collect fluids (e.g., blood), secretions and/or air during controlled aspiration of the pleural cavity and/or mediastinum. The device typically
| Company | Devices | Share |
|---|---|---|
| Teleflex Incorporated | 65 | 81% |
| Alleva Medical Limited | 8 | 10% |
| Atrium Medical Corporation | 4 | 5% |
| Solomed, S.A. De C.V. | 2 | 2% |
| Pacific Hospital Supply Company Limited | 1 | 1% |
Company = labeler of record on GUDID. 5 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 |
|---|---|---|
| KDQ | BOTTLE, COLLECTION, VACUUM | 53 |
| KDQ | Bottle, Collection, Vacuum | 16 |
| CAC | Apparatus, autotransfusion | 12 |
| CAC | APPARATUS, AUTOTRANSFUSION | 9 |
Use these as the dimensions to specify in a tender line.
80 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Thoracic suction collection container", from 5 companies. The largest labeler is Teleflex Incorporated with 81% of records.
KDQ (BOTTLE, COLLECTION, VACUUM), KDQ (Bottle, Collection, Vacuum), CAC (Apparatus, autotransfusion), CAC (APPARATUS, AUTOTRANSFUSION)
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.