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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

LID for SPRI basket 585x395 — Class I MDR by Harry Holms AB

MD Atlas
Harry Holms AB

EUDAMED last updated this device on Jan 25, 2022

LID for SPRI basket 585x395

7350125440007T

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Harry Holms AB
UDI-DI code: 07350125440438
Reference / catalog number: 705550

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View device family (Basic UDI)

Manufacturer information

Organization name: Harry Holms AB
SRN: SE-MF-000001907
Manufacturer status: Active

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500557350125440007TOn the market 500547350125440007TOn the market Inner Lid for Instrument Tray SPRI I 437x3277350125440007TOn the market Inner Lid for Instrument Tray SPRI II 327x2377350125440007TOn the market Inner Lid for Instrument Tray SPRI III 237x1577350125440007TOn 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

No critical warnings reported for this device.

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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: LID for SPRI basket 585x395
UDI-DI code: 07350125440438
Basic UDI-DI: 7350125440007T
Reference / catalog number: 705550
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 585 MU50
395 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07350125440438

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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.

S010401TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS

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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