Primary Device ID | 01836230004056 |
NIH Device Record Key | ef17b60a-a610-43a9-ab6a-8353dffb1a3c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Protective Cover 100/100cm |
Version Model Number | 5021 |
Company DUNS | 532186541 |
Company Name | PHARMA SEPT MEDICAL PRODUCTS (1995) LTD. |
Device Count | 1 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00836230004057 [Primary] |
GS1 | 01836230004056 [Package] Contains: 00836230004057 Package: box [15 Units] In Commercial Distribution |
GS1 | 02836230004055 [Package] Package: box [4 Units] In Commercial Distribution |
KQM | Camera, Surgical And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-23 |
Device Publish Date | 2022-11-15 |
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