DLINE "Light body C-Silicone"

Organization name

UAB "Medicinos linija"

SRN

LT-MF-000002719

Manufacturer status

Active

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

• CW449

  EUDAMED did not publish a description for this code.
• CW206

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

  EUDAMED did not publish a description for this code.
• CW009

  EUDAMED did not publish a description for this code.
• CW038

  EUDAMED did not publish a description for this code.
• CW296

  EUDAMED did not publish a description for this code.
• CW193

  EUDAMED did not publish a description for this code.
• CW401

  EUDAMED did not publish a description for this code.
• CW406

  EUDAMED did not publish a description for this code.

Primary placement in Lithuania; available across 1 country total.

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

Trade name

DLINE "Light body C-Silicone"

UDI-DI code

04772178005380

Basic UDI-DI

4772178ML07IMTS

Reference / catalog number

24221

Issuing entity

GS1

Risk category

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

i-MPRESS Putty, i-MPRESS Light Body and i-MPRESS Universal Activator are condensation type silicone impression materials with perfect balance between rigidity and elasticity. May be used with all types of impression trays. Do not require special treatment before use.

Additional information URL

https://www.dline.ee/eIFU

Clinical sizes

No clinical sizes registered for this device.

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

• Q01020104DENTAL IMPRESSION SILICONES