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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

20.100.35 — Class I MDD by SpineSave AG

MD Atlas
SpineSave AG

EUDAMED last updated this device on May 27, 2024

20.100.35

B-04260682510679

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: SpineSave AG
UDI-DI code: 04260682510679
Reference / catalog number: 20.100.35

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Manufacturer information

Organization name: SpineSave AG
SRN: CH-MF-000041640
Manufacturer status: Active

Related devices

20.012.03B-04260682510556On the market 20.006.00B-04260682510389On the market 20.013.02B-04260682510587On the market 20.004.00B-04260682510334On the market 20.005.10B-04260682510372On 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 Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04260682510679
Basic UDI-DI: B-04260682510679
Reference / catalog number: 20.100.35
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 5.4 MU50

EMDN nomenclature code(s)

L098003ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY TAPS, 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification