- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jan 17, 2025
376034811400.09CJPrimary 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 RECTAL STRAW 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 Austria. 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 →03760348110140Basic 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 →376034811400.09CJRK-75UDI 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)03760348110140
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 - ACCESSORIESSterile
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 →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Austria; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Nov 24, 2024 | Still on market |
| France | Feb 28, 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 →376034811200.02BAOn the marketSTARFIT NASOGASTRIC FEEDING TUBE WITH GUIDEWIRE NGG10-92376034811200.02BAOn the marketSTARFIT NASOGASTRIC FEEDING TUBE WITH GUIDEWIRE NGG12-120376034811200.02BAOn the marketSTARFIT RECTAL STRAW 150 MM RK150376034811400.09CJOn the marketSTARFIT SAMPLING STRAW SS01376034811400.03C6On the marketSTARFIT UNVERSAL BOTTLE ADAPTOR UBA01376034811400.06CCOn the market