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EUDAMED last updated this device on Jul 31, 2026
692303342021010064014ZBlood Collection Sampling Holder is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Zhejiang Kindly Medical Devices Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
069230334216560110109-012 packaging levels registered — each level carries its own UDI-DI.
06923033421656× 1 unitBase unit16923033421653× 100 units26923033421650× 20 units(01)06923033421656
European Medical Device Nomenclature — the EU product classification assigned to this device.
A01018001HOLDERS FOR COLLECTION NEEDLESCN-MF-000007594The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jul 31, 2026 | Jul 30, 2031 |
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.
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 →No certificate specifically references this device's Basic UDI-DI.
69230334202002a00801MLOn the marketBlood Collecting Needle(visible flashback type)69230334202002a00801MLOn the marketBlood Collecting Needle(visible flashback type)69230334202002a00801MLOn the marketBlood-collecting needles69230334202002a00801MLOn the marketDispensing needle (with filtering membrane)69230334202102a04401NKOn the marketDispensing needle (without filtering membrane))69230334202102a04401NKOn 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.