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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

ADSON STILLE ARTERY FORCEPS — Class I MDD by Stille AB

MD Atlas
Stille AB

EUDAMED last updated this device on Mar 29, 2023

ADSON STILLE ARTERY FORCEPS

B-07332339211561

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Stille AB
UDI-DI code: 07332339211561
Reference / catalog number: 103-10262-191

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View device family (Basic UDI)

Manufacturer information

Organization name: Stille AB
SRN: SE-MF-000001228
Manufacturer status: Active

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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.

Critical warnings

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

CW018
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Sweden; available across 1 country total.

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

Device identification

Trade name: ADSON STILLE ARTERY FORCEPS
UDI-DI code: 07332339211561
Basic UDI-DI: B-07332339211561
Reference / catalog number: 103-10262-191
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: curved 19 cm 7.5 in
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 19 MU10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

L031306HEMOSTATIC FORCEPS, REUSABLE

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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