Primary Device ID | 27290109154866 |
NIH Device Record Key | cd49fe91-bf5b-4f21-b035-75ee92d99792 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AP 223-01 MICROBORE ADMINISTRATION SET WITH VENTED/NON-VENTED SPIKE, |
Version Model Number | 12003-000-0033 |
Company DUNS | 533108028 |
Company Name | EITAN MEDICAL LTD |
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 | 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 | 17290109154869 [Primary] |
GS1 | 27290109154866 [Package] Contains: 17290109154869 Package: Cardboard box [30 Units] In Commercial Distribution |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-22 |
Device Publish Date | 2023-03-14 |
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