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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

XBX1201100-VTAF 000200 — Class I MDR by Stiplastics

MD Atlas
Stiplastics

EUDAMED last updated this device on Oct 17, 2023

XBX1201100-VTAF 000200

37011717CG1P9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Stiplastics
UDI-DI code: 03701171702515
Reference / catalog number: XBX1201100-VTAF 000200

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Manufacturer information

Organization name: Stiplastics
SRN: FR-MF-000000826
Manufacturer status: Active

Related devices

Hemobox37011717PANSJKOn the market Hemobox37011717COTONF2On the market 05AC158 400100 37011717KITHYGIENE2WOn the market 05AC158 30017037011717KITHYGIENE2WOn the market 05AC158 20019037011717KITHYGIENE2WOn the market

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.

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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: not provided
UDI-DI code: 03701171702515
Basic UDI-DI: 37011717CG1P9
Reference / catalog number: XBX1201100-VTAF 000200
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: 2000
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification