Peakmed central venous catheter kit
SCORP MEDITECH LTD
VALID
Registration Information
- Device ID
- 21091
- Registration Number
- MD/2026/279
- Registration Year
- 2026
- Retention Year
- 2026
Device Information
- Device Tradename
- Peakmed central venous catheter kit
- Licence Status
- VALID
- WIPO NCL Match
- No automatic WIPO basic-number match has been persisted for this device yet.
Manufacturer Information
- Manufacturer
- SCORP MEDITECH LTD
- Local Technical Representative
- SCORP MEDITECH LTD
Record Information
- Last Fetched
- 2026-05-04 08:22:50
- Last Updated
- 2026-11-09 08:02:00
Important Notice
Registration information is sourced from the Pharmacy and Poisons Board of Kenya. Classification references are sourced from WIPO Nice Classification Publication (NCLPUB): https://nclpub.wipo.int/enfr/. Always verify critical records with official authorities before procurement.