CANNEFF

Organization name

CB21 Pharma, s.r.o.

SRN

CZ-MF-000037413

Manufacturer status

Active

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

• CW999

  Keep away from children. Do not take the suppositories by mouth. Do not use after expiration date or in case the packaging is opened or damaged.

Primary placement in Czechia; available across 10 countries total.

Trade name

CANNEFF

UDI-DI code

859419703041SUP6F

Basic UDI-DI

B-859419703041SUP6F

Reference / catalog number

CANNEFF SUP – rectal suppositories

Issuing entity

HIBCC

Risk category

Class IIb

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.

• G05TOPICAL ANORECTAL ADMINISTERED GASTRO-INTESTINAL SYSTEM DEVICES

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

Certificate health across this manufacturer's portfolio.