- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Apr 1, 2024
B-TR01002AASTNEODRAP ® Universal pack set 2AA is an MDD-legacy medical device registered in EUDAMED. It is classified as Class I. Manufactured by Adhe-Els SA.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-TR01002AASTTR01002AAD-TR01002AAST
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
T0202SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS)5 warnings recorded — scroll inside the panel to see all entries.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | May 25, 2021 | May 26, 2024 |
TN-MF-000011757543722 MR2Sterile
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 DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic 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 →UDI 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 →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 →B-KIT-009BCSOn the marketNEODRAP ® Universal pack set 2B-TR01002S2On the marketNEODRAP ® Universal pack set 2AB-TR01002A9COn the marketNEODRAP ® Universal pack set 2BB-TR01002B9EOn the marketNEODRAP® Adhesive tape set 10x50cmB-KIT-010BC4On the marketNEODRAP® Anesthesia set Set 23B-KIT-023UZOn the marketNo certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.No certificate specifically references this device's Basic UDI-DI.