RetraLight

Organization name

PulseLavage AB

SRN

SE-MF-000002363

Manufacturer status

Active

3 warnings recorded — scroll inside the panel to see all entries.

• CW009

  EUDAMED did not publish a description for this code.
• CW001

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.

Primary placement in Sweden; available across 3 countries total.

Trade name

RetraLight

UDI-DI code

07350093650600

Basic UDI-DI

B-07350093650600

Reference / catalog number

RL4001

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• K01020106MINIMALLY INVASIVE SURGERY SPREADERS AND RETRACTORS, SINGLE-USE

Certificate health across this manufacturer's portfolio.