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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

MACOSEAL twin EVA minibag — Class I MDR by Conroy Medical AB

MD Atlas
Conroy Medical AB

EUDAMED last updated this device on Jul 11, 2025

MACOSEAL twin EVA minibag

735011599102AD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Conroy Medical AB
UDI-DI code: 07350115990134
Reference / catalog number: 9MSL3622

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View device family (Basic UDI)

Manufacturer information

Organization name: Conroy Medical AB
SRN: SE-MF-000027430
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
Identified areas are included in the IFU

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Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: MACOSEAL twin EVA minibag
UDI-DI code: 07350115990134
Basic UDI-DI: 735011599102AD
Reference / catalog number: 9MSL3622
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: MACOSEAL twin EVA minibag is an automatic system for sealing ethylene vinyl acetate (EVA) tubes, especially for tubes in blood pack systems. MACOSEAL twin EVA minibag creates a distinct sealing pattern, resulting in segments that can be separated with no damage to the blood inside the tubes. Tubing segments may be formed by inserting the tubing into the slot at the front of the hand unit to create a series of seals.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07350115990134

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

No 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.