- Role
- Country
- Date of registration
- Address
TH-MF-000010448SRI TRANG GLOVES VIVA LITE NITRILE POWDER-FREE EXAMINATION GLOVES is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Sri Trang Gloves (Thailand) Public Company Limited. Placed on the EU market in Croatia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jan 29, 2025
88591306NO02VRPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08859130622154
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
Contains Dithiocarbamates which could lead to allergic reaction - do not use, if sensitized.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Croatia; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| CroatiaPrimary placement | — | Still on market |
| Austria | — | Still on market |
| Belgium | — | Still on market |
| Bulgaria | — | Still on market |
| Cyprus | — | Still on market |
| Czechia | — | Still on market |
| Germany | — | Still on market |
| Denmark | — | Still on market |
| Estonia | — | Still on market |
| EL | — | Still on market |
| Spain | — | Still on market |
| Finland | — | Still on market |
| France | — | Still on market |
| Hungary | — | Still on market |
| Ireland | — | Still on market |
| Iceland | — | Still on market |
| Italy | — | Still on market |
| Liechtenstein | — | Still on market |
| Lithuania | — | Still on market |
| Luxembourg | — | Still on market |
| Latvia | — | Still on market |
| Malta | — | Still on market |
| Netherlands | — | Still on market |
| Norway | — | Still on market |
| Poland | — | Still on market |
| Portugal | — | Still on market |
| Romania | — | Still on market |
| Sweden | — | Still on market |
| Slovenia | — | Still on market |
| Slovakia | — | Still on market |
| Türkiye | — | Still on market |
| XI | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08859130622154Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
88591306NO02VRDNOFLOGUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
1 packaging level registered — each level carries its own UDI-DI.
08859130622154× 180 unitsBase unit18859130622151× 10 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
T01020204NITRILE EXAMINATION / TREATMENT GLOVES88591306NO02VROn the marketSRI TRANG GLOVES VIVA LITE NITRILE POWDER-FREE EXAMINATION GLOVES88591306NO02VROn the marketSRI TRANG GLOVES VIVA LITE NITRILE POWDER-FREE EXAMINATION GLOVES88591306NO02VROn the marketSRI TRANG GLOVES VIVA LITE NITRILE POWDER-FREE EXAMINATION GLOVES88591306NO02VROn the marketSRI TRANG GLOVES VIVA LITE NITRILE POWDER-FREE EXAMINATION GLOVES88591306NO02VROn the marketSRI TRANG GLOVES VIVA LITE NITRILE POWDER-FREE EXAMINATION GLOVES88591306NO02VROn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
G15 099188 0014IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →