A slender, double-ended, hand-held manual surgical instrument intended to be used to explore and examine wounds, and additionally to introduce and pack gauze or dressings into the wound. It consists of a flat blunt blade at one end and a packer at the other en
| Company | Devices | Share |
|---|---|---|
| Rz-Medizintechnik Gmbh | 69 | 76% |
| American Medicals | 6 | 7% |
| The Trustee For Kaiser Family Trust | 5 | 5% |
| Robinson Healthcare Limited | 3 | 3% |
| Arthrex, Inc. | 3 | 3% |
| Fentex Medical Gmbh | 2 | 2% |
| American Medical Endoscopy, Inc. | 1 | 1% |
| Med Saver, Inc. | 1 | 1% |
| Sklar Corporation | 1 | 1% |
Company = labeler of record on GUDID. 9 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 |
|---|---|---|
| MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE | 45 |
| HXB | PROBE | 9 |
| KAK | PROBE, ENT | 8 |
| KAK | Probe, Ent | 5 |
| GZX | INSTRUMENT, MICROSURGICAL | 4 |
| HXB | Probe | 4 |
Use these as the dimensions to specify in a tender line.
91 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "General surgery wound probe/packer", from 9 companies. The largest labeler is Rz-Medizintechnik Gmbh with 76% of records.
MDM (INSTRUMENT, MANUAL, SURGICAL, GENERAL USE), HXB (PROBE), KAK (PROBE, ENT), KAK (Probe, Ent)
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.