Obturator f. resectoscope sheath (standard)

Organization name

Erbe Vision GmbH

SRN

DE-MF-000010268

Manufacturer status

Active

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

• CW133

  "The devices are contraindicated for all the intended uses, other than the ones claimed by manufacturer. The devices are to be neither used in contact with central circulatory system nor with central nervous system. Do not use the devices if one condition is present: • Acute inflammation of the abdominal area • Urinary tract infection • Coagulation disorder"

Primary placement in Germany; available across 1 country total.

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

Trade name

Obturator f. resectoscope sheath (standard)

UDI-DI code

04260214652150

Basic UDI-DI

426021465OBTURATORSA5

Reference / catalog number

20862-035

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

Obturator f. resectoscope sheath 24CH/26CH

Additional information URL

https://register.erbe-med.com/productfinder/Marketingmaterialien/30864-001_ERBE_EN_Endoscopy_Instruments_&_Accessories__D209851.pdf

Clinical sizes

• 24–26 MU170

• Z12020780GENITOURINARY ENDOSCOPY INSTRUMENTS - HARDWARE ACCESSORIES

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