Primary Device ID | 44710810100800 |
NIH Device Record Key | 013bd926-8578-4a56-aa77-26aa281f20c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Babi.Plus |
Version Model Number | BC23-HD |
Catalog Number | 12.5 cm H2O Pressure Relief Manifold with Gas Supp |
Company DUNS | 656854379 |
Company Name | GALEMED CORPORATION |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 04710810100802 [Primary] |
GS1 | 24710810100806 [Package] Contains: 04710810100802 Package: Box [12 Units] In Commercial Distribution |
GS1 | 44710810100800 [Package] Contains: 24710810100806 Package: Carton [2 Units] In Commercial Distribution |
BZD | Ventilator, Non-Continuous (Respirator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |
44710810093577 | BC01-AU |
44710810119741 | B024 |
44710810119734 | B023 |
44710810119727 | B022 |
44710810119710 | B021 |
44710810119703 | B020 |
44710810100800 | Distributed by Teleflex |
44710810100794 | Distributed by Teleflex |
04710810093579 | BC01-AU |
44710810093560 | BC23-AU |
44710810117525 | PA01 |
44710810093553 | BC51-AU |
04710810105265 | BC01-AU |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BABI.PLUS 77642836 3764949 Live/Registered |
GALEMED CORPORATION 2009-01-03 |