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RZ Medizintechnik GmbH

RZ-Medizintechnik GmbH · Model 253-000-319 · UDI-DI 04049197515399

FAJ Prescription
1
510(k) clearances
10,639
Adverse events (3 deaths)
22
Recalls
137
Facilities

Description

Laser working element Standard Lock for 2.9mm scopes, for use with 22FR 0.8mm fibers, with push button (stop)

Recalls

DateFirmReason
2023-12-04Shirakawa Olympus Co., Ltd.Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
2023-12-04Shirakawa Olympus Co., Ltd.Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
2023-12-04Shirakawa Olympus Co., Ltd.Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
2023-12-04Shirakawa Olympus Co., Ltd.Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
2023-12-04Shirakawa Olympus Co., Ltd.Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
2023-12-04Shirakawa Olympus Co., Ltd.Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
2023-09-25Aizu Olympus Co., Ltd.Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endo
2022-05-03Karl Storz EndoscopyThe endoscope may experience a loss of image when activating monopolar electrocautery, due a manufacturing assembly process issue.
2022-04-20Olympus Corporation of the AmericasIncorrect adhesive used to secure the diopter ring and nameplate ring. Improperly connected diopter ring may result in the loss of adjustment function leading to a blurred field of
2022-04-01Karl Storz EndoscopyFailure to achieve the expected six-log reduction in microorganisms following the disinfection process.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.