Medical device licence · 539 · Class 3
PROPLAST II IMPLANTS
No longer licensed: cancelled: renewal not answered
Licence status Cancelled: renewal not answered; first licensed February 16, 1999; ended April 14, 2000. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 539
- Licence holder
- Genatis Biofunctional Tech. Sa.Nyon, VD, Switzerland
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Family
- First licensed
- February 16, 1999
- Ended
- April 14, 2000
- Devices covered
- 14
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- PROPLAST II CHIN
- PROPLAST II GIEDROJC DORSAL COLUMELLA
- PROPLAST II HINDERER TYPE MALAR
- PROPLAST II LARGE BLOCK
- PROPLAST II NASAL DORSUM
- PROPLAST II OTOPLASTY
- PROPLAST II PERI-ORBITAL RIM
- PROPLAST II SHEEN PRE-MAXILLARY
- PROPLAST II SHEETING
- PROPLAST II SMALL BLOCK
- PROPLAST II WHITAKER MALAR
- PROPLAST II WHITAKER MANDIBLE LEFT, RIGHT
- PROPLAST II ZYGOMATIC NOTCHED LEFT, RIGHT
- PROPLAST II ZYGOMATIC/LATERAL ORBITAL RIM
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.