A compact metal rod intended to be used during expansion of a laparoscopic access port (e.g., from 10 to 20 mm) by facilitating: 1) removal of an existing access cannula; and 2) introduction of a dilator/cannula assembly. It is inserted into the existing acces
| Company | Devices | Share |
|---|---|---|
| Aesculap Ag | 37 | 63% |
| Aesculap, Inc. | 11 | 19% |
| Sontec Instruments, Inc. | 5 | 8% |
| Cutting Edge Spine, Llc | 3 | 5% |
| Richard Wolf Gmbh | 1 | 2% |
| Gimmi Gmbh | 1 | 2% |
| Integra Lifesciences Production Corporation | 1 | 2% |
Company = labeler of record on GUDID. 7 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 |
|---|---|---|
| GCJ | Laparoscope, general & plastic surgery | 50 |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 10 |
| LXH | Orthopedic manual surgical instrument | 6 |
| NBH | Accessories, arthroscopic | 1 |
| DXC | CLAMP, VASCULAR | 1 |
Use these as the dimensions to specify in a tender line.
59 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Laparoscopic dilation guide rod", from 7 companies. The largest labeler is Aesculap Ag with 63% of records.
GCJ (Laparoscope, general & plastic surgery), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT), LXH (Orthopedic manual surgical instrument), NBH (Accessories, arthroscopic)
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.