A connecting device intended to join two incompatible devices/components through a system of uniquely coded pins, slots, or holes which match when united, and provide security against the inadvertent coupling of devices other than a specific pair. The device i
| Company | Devices | Share |
|---|---|---|
| Superior Products, Llc | 98 | 42% |
| Richard Wolf Gmbh | 32 | 14% |
| Conmed Corporation | 26 | 11% |
| Western Enterprises | 25 | 11% |
| Bay Corporation | 17 | 7% |
| Karl Storz Gmbh & Co. Kg | 11 | 5% |
| T.A.G Medical Products Agricultural Cooperative Association | 7 | 3% |
| Advanced Neuromodulation Systems, Inc. | 4 | 2% |
| St. Jude Medical, Inc. | 3 | 1% |
| Drägerwerk Ag & Co. Kgaa | 2 | 1% |
| Beijing Ruicheng Medical Supplies Co., Ltd. | 2 | 1% |
| Shanghai Draeger Medical Instrument Co.,Ltd. | 1 | 0% |
Company = labeler of record on GUDID. 17 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 |
|---|---|---|
| CAM | YOKE ASSEMBLY, MEDICAL GAS | 98 |
| CAM | Yoke Assembly, Medical Gas | 42 |
| MKJ | Automated external defibrillators (non-wearable) | 28 |
| MKJ | Automated External Defibrillators (Non-Wearable) | 27 |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 18 |
| LDD | Dc-defibrillator, low-energy, (including paddles) | 10 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
233 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Pin-indexed adaptor, reusable", from 17 companies. The largest labeler is Superior Products, Llc with 42% of records.
CAM (YOKE ASSEMBLY, MEDICAL GAS), CAM (Yoke Assembly, Medical Gas), MKJ (Automated external defibrillators (non-wearable)), MKJ (Automated External Defibrillators (Non-Wearable))
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.