Home › Carl Zeiss Meditec AG › ZEISS CONNECT
ZEISS CONNECT
Carl Zeiss Meditec AG · Model 2.0 · UDI-DI 04049539070135
10
510(k) clearances
672
Adverse events
14
Recalls
195
Facilities
Description
The ZEISS® Connect App mobile application will be an optional accessory of ZEISS® UNO 3 microscope product. ZEISS® Connect application SW will be available to the end user as an iOS app and user should be able to download and install the same from Apple App store. ZEISS® Connect App will pair wirelessly to the UNO3 variants of microscope and associated peripheral devices (like monitor etc.). This database entry covers UDI for SW version 2.0 and higher. Version 2.0-> UDI - (01)04049539070135(10)200-> Version 3.0-> UDI - (01)04049539070135(10)301 ->Version 4.2-> UDI - (01)04049539070135(10)420
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-23 | Steris Corporation | This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configura |
| 2024-06-04 | Baxter Healthcare Corporation | Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products l |
| 2023-12-20 | Barco N.V. | Barco became aware of a problem with I2C cables in the manufacturing process of a limited batch of MDSC-85xx NXF products. The functionality of the built-in MNA decoder is blocked |
| 2015-05-28 | Barco Inc. | User settings were no longer on the monitor's memory after these systems were powered off and back on. |
| 2015-03-05 | Sony Latin America | Monitor has either not turned on or has lost image during clinical use. |
| 2013-03-18 | Linvatec Corp. dba ConMed Linvatec | The VP1600 HD Still Capture Image System is recalled due to an anomaly between the software code in the VP1600 console and the communications interface for various keyboard key str |
| 2010-10-25 | Mako Surgical Corporation | MAKO Surgical Corporation recalled ONE infra-red camera MAKO PN 204854 which was a component of their RIO Robotic Arm Interactive Orthopedic System with SSN P7-03127, on November 2 |
| 2010-09-17 | Linvatec Corp. dba ConMed Linvatec | If the VHM Arm is left in the locked position, the gas spring can lose pressure and releasing the lock can result in a sudden downward movement. |
| 2010-02-23 | Linvatec Corp. dba ConMed Linvatec | ConMed Linvatec, Endoscopy Division, dba. ConMed Linvatec, Largo, Florida is recalling five products: (1.) Video Cart Premium 120 VAC (VP6501), (2.) Video Cart Multi-Specialty 120 |
| 2010-02-23 | Linvatec Corp. dba ConMed Linvatec | ConMed Linvatec, Endoscopy Division, dba. ConMed Linvatec, Largo, Florida is recalling five products: (1.) Video Cart Premium 120 VAC (VP6501), (2.) Video Cart Multi-Specialty 120 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.