- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jan 28, 2025
376034811400.02C4Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →STARFIT ENTERAL MILK STRAW MS01 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by HOIST MEDICAL . Placed on the EU market in Romania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →03760348110171Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →376034811400.02C4MS01UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →(01)03760348110171
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
G0280GASTROINTESTINAL TUBES - ACCESSORIES2 warnings recorded — scroll inside the panel to see all entries.
CW009CW007Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary placement in Romania; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| RomaniaPrimary placement | Jan 27, 2025 | Still on market |
FR-MF-000026140Certificate health across this manufacturer's portfolio.
1000217799IssuedNotified 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 →1000217799376034811100.01ATOn the marketPURFIT GASTROSTOMY BUTTON 14FR 3.5 CM PGB14-3.5376034811100.01ATOn the marketPURFIT GASTROSTOMY BUTTON 14FR 3CM PGB14-3.0376034811100.01ATOn the marketPURFIT GASTROSTOMY BUTTON 14FR 4 CM PGB14-4.0376034811100.01ATOn the marketPURFIT GASTROSTOMY BUTTON 14FR 5 CM PGB14-5.0376034811100.01ATOn the market