8203

Organization name

EM EXACT, S.A.

SRN

ES-MF-000010830

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  The use of the products is contraindicated in the case of patients with conditions that rule out the use of surgery for the placement of dental implants. The use of the products is contraindicated in the case of patients in whom the desired sizes, numbers or positions of the implants cannot be achieved to achieve a safe support of functional or possibly parafunctional loads. These products should not be used on patients sensitive to their raw materials: Titanium, Chrome-Cobalt or Peek.

Primary placement in Spain; available across 2 countries total.

Trade name

not provided

UDI-DI code

08445594017454

Basic UDI-DI

8445594_TORN_RECT_LQ

Reference / catalog number

8203

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

MDR [Regulation (EU) 2017/745 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.

• P01020180DENTAL IMPLANTS - ACCESSORIES