Primary Device ID | 04049539101952 |
NIH Device Record Key | a7dea1d8-1d79-4a9f-816f-ad0007082366 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Foot Switch Drapes |
Version Model Number | 326012-0000-000 |
Company DUNS | 342228620 |
Company Name | Carl Zeiss Meditec AG |
Device Count | 50 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Height | 24 Inch |
Width | 14 Inch |
Height | 61 Centimeter |
Width | 36 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049539101143 [Unit of Use] |
GS1 | 04049539101952 [Primary] |
GS1 | 04049539102164 [Package] Package: [4 Units] In Commercial Distribution |
KKX | Drape, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-22 |
Device Publish Date | 2016-08-22 |
04049471100143 - Treatment Pack (Size M) | 2024-02-19 single use accessory for ZEISS femtosecond lasers |
04049471100150 - Treatment Pack (Size L) | 2024-02-19 single use accessory for ZEISS femtosecond lasers |
04049471100167 - Treatment Pack (Type KP) | 2024-02-19 single use accessory for ZEISS femtosecond lasers |
04049471100136 - Treatment Pack (Size S) | 2024-02-16 single use accessory for ZEISS femtosecond lasers |
04049539101341 - EyeMag Smart | 2023-11-16 |
04049539101358 - EyeMag Pro S | 2023-11-16 |
04049539101365 - EyeMag Pro F | 2023-11-16 |
04049539064103 - PENTERO® 800 S | 2023-09-19 |