Primary Device ID | 04049539104359 |
NIH Device Record Key | c4634495-f4cd-4bc9-a7a3-1eafbfb0a104 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | YELLOW 560 |
Version Model Number | 302582-9205-000 |
Company DUNS | 342228620 |
Company Name | Carl Zeiss Meditec AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049539104359 [Primary] |
IZI | System, X-Ray, Angiographic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-21 |
Device Publish Date | 2018-02-16 |
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