Devices (same UDI-DI)
1
Certificates
1
Countries
2
Notified Bodies
1
Let the assistant research this device
The Research Assistant compiles risk class, certificates, notified bodies and related records — and cites every one.
Free to try · every answer cites its records
Basic Information
- Primary DI
- 08906062420218
- Basic UDI-DI Code
- B-08906062420218
- Reference
- S30020
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- Multimedics LLP
Additional Description
The M’Sure-S Sirolimus eluting stent system is a combination product comprised of two regulated components: a device (a coronary stent system) and a drug product (a formulation of Sirolimus contained in a polymer coating) pre mounted on balloon catheter between two platinum iridium radio opaque marker bands.
CND Nomenclature Codes
| Code | Description |
|---|---|
| P070402010301 | CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II Section 4 | 10000351742-PA-NA-IND | DNV Product Assurance AS | Expired |
Available In Countries
🇨🇿 Czechia
🇹🇷 Türkiye
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDD).
SafeSept Transseptal Guidewire
Device
EU MDD
·
Eu Md Class 3
·Pressure Products Medical Device Manufacturing LLC.·On the market·32 countries
PTCA BALLOON DILATION CATHETERS
Device
EU MDD
·
Eu Md Class 3
·BrosMed Medical Co., Ltd·On the market·32 countries
PTCA BALLOON DILATION CATHETERS
Device
EU MDD
·
Eu Md Class 3
·BrosMed Medical Co., Ltd·On the market·32 countries
Cutanplast Standard
Device
EU MDD
·
Eu Md Class 3
·Mascia Brunelli S.p.A.·On the market·21 countries
PTCA BALLOON DILATION CATHETERS
Device
EU MDD
·
Eu Md Class 3
·BrosMed Medical Co., Ltd·On the market·32 countries
PTCA BALLOON DILATION CATHETERS
Device
EU MDD
·
Eu Md Class 3
·BrosMed Medical Co., Ltd·On the market·32 countries