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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

734974 — Class IIa MDR by Laboratorios Grifols S.A.

MD Atlas
Laboratorios Grifols S.A.

EUDAMED last updated this device on Nov 25, 2025

734974

8437017294A060001MU

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratorios Grifols S.A.
UDI-DI code: 08437017294122
Reference / catalog number: 734974

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Manufacturer information

Organization name: Laboratorios Grifols S.A.
SRN: ES-MF-000000767
Manufacturer status: Active

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Critical warnings

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

CW999
- Do not re-use. -The product reuse poses risk of infection. -Do not use if package is damaged. -The sterile barrier system is the product itself. -The scales included are indicative. -Once used, discard the product following the centre protocol.

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Jun 19, 2025	Still on market
Portugal	Jul 16, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437017294122
Basic UDI-DI: 8437017294A060001MU
Reference / catalog number: 734974
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: The medical device Vacuflasc is a sterile and non-pyrogenic product consisting of a Type I glass bottle, hermetically sealed with an halogenated butyl rubber stopper and an aluminum tear-off capsule, inside of which the vacuum has been made.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A0601010102DRAINAGE SYSTEMS WITH RESERVOIR

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.