BIP Foley Catheter 3-way, 22 Ch/Fr, 30ml/cc

Organization name

Bactiguard AB

SRN

SE-MF-000020790

Manufacturer status

Active

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

• CW999

  Under the following conditions the use of the device should be avoided, unless justified by the treating physician: For urethral catheterization:  Trauma of urethra or bladder  Acute prostatitis  Allergy or sensitivity to latex
• CW999

  Under the following conditions the use of the device should be avoided, unless justified by the treating physician: For suprapubic catheterization:  Known or suspected carcinoma of the bladder  Absence of an easily palpable or ultrasonographically localized distended urinary bladder  Previous lower abdominal surgery  Coagulopathy (until the abnormality is corrected)  Ascites  Prosthetic devices in lower abdomen (e.g., hernia mesh)  Allergy or sensitivity to latex

Primary placement in Sweden; available across 1 country total.

Trade name

BIP Foley Catheter 3-way, 22 Ch/Fr, 30ml/cc

UDI-DI code

07333330104944

Basic UDI-DI

7333330FOLEYLATUV110301Z9

Reference / catalog number

112223010

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

The BIP Foley catheter is sterile, single use, disposable urethral catheter of Foley type. The BIP Foley Catheter is made of natural rubber latex that is coated with the Bactiguard® coating and hydrophilic coating. The Bactiguard® coating consists of an alloy of noble metals that reduces adhesion and colonization of microorganisms (e.g. bacteria) on the surface of the catheter. The hydrophilic coating offers excellent lubrication for improved patient comfort during use. The BIP Foley Catheter has good tissue friendliness.

Additional information URL

https://www.bactiguard.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.

• U010299URETHRAL PROSTATIC AND BLADDER CATHETERS, WITH BALLOON - OTHER

Certificate health across this manufacturer's portfolio.