Eu Mdd Eu Md Class 3 On The Market 🇸🇪 Sweden

CARTINORM

Bohus BioTech AB · 🇸🇪 Sweden
Devices (same UDI-DI)
1
Certificates
3
Countries
2
Notified Bodies
3

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Basic Information

Primary DI
17350030051955
Basic UDI-DI Code
B-17350030051955
Reference
-
Device Types
Single use Sterile
Regulation
Eu Mdd
Classification
Eu Md Class 3
Status
On The Market
Manufacturer
Bohus BioTech AB

Additional Description

Cartinorm®(sodium hyaluronate) is a 1.0% viscoelastic, sterile and clear single dose solution for injection into the joint cavity. The highly purified sodium hyaluronate is dissolved in a physiological buffer at pH 6.8-7.6.

CND Nomenclature Codes

Code Description
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES

Certificates

Type Number
MDD Annex II (excluding section 4) D1001800117
MDD Annex II Section 4 D1001800097
MDD Annex II (excluding section 4) D1001800076

Available In Countries

🇩🇪 Germany 🇭🇺 Hungary

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