REMOVER_50

Organization name

Synkotech Biocompatible Materials S.L

SRN

ES-MF-000031010

Manufacturer status

Active

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

• CW262

  Single patient multiple use
• CW057

  Highly flammable liquid and vapour.
• CW010

  Avoid contact with eyes; in case of contact, rinse immediately with water. If the product comes into contact with an open wound, rinse with water. Discontinue use if irritation or an allergic reaction occurs. A patch test on a small area of skin may be performed prior to use. Keep out of reach of children.
• CW007

  Do not use if package is damaged
• CW135

  Keep out of reach of children.

Primary placement in Spain; available across 1 country total.

Trade name

not provided

UDI-DI code

08437025406241

Basic UDI-DI

8437025406SRHV

Reference / catalog number

REMOVER_50

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

Eliminador de Adhesivo médico

Additional information URL

https://synkotechbio.com/

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.

• M9003SOLUTIONS FOR ADHESIVE TAPE REMOVAL