Medical device licence · 93638 · Class 2
DIO SURGICAL KIT
Yes: licensed in Canada
Licence status Issued (active); first licensed July 25, 2014. It is in Health Canada’s list of active licences.
- Licence number
- 93638
- Licence holder
- Dio CorporationBusan, South Korea
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Group Family
- First licensed
- July 25, 2014
- Devices covered
- 25
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- BONE EXPENDER KIT
- DIO BONE EXPANDER KIT
- DIO MASTER S KIT
- DIO MIT KIT
- DIONAVI PROTEM SURGICAL KIT
- DIONAVI. SURGICAL GUIDE FIX KIT
- DIONAVI. SURGICAL KIT
- DIONAVI. UF MASTER KIT
- DIONAVI. UF STARTER KIT
- DIONAVI. UF(II) NARROW SURGICAL KIT
- DR. SOS KIT
- OSTEOTOME KIT
- PROSTHETIC KIT
- PROTEM SURGICAL KIT
- SINUS KIT
- UF MASTER KIT
- UF STARTER KIT
- UF SURGICAL KIT
- UF(II) IMPLANT SYSTEM KIT
- UF(II) INTERNAL MASTER KIT
- UF(II) MASTER KIT
- UF(II) NARROW IMPLANT SYSTEM KIT
- UF(II) NARROW SURGICAL KIT
- UF(II) SURGICAL KIT
- UF(II) WIDE SURGICAL KIT
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.