Primary Device ID | 50860000082803 |
NIH Device Record Key | 94c50a53-3e7a-4f95-bd41-a90fa118368f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | G.E.B. tubing |
Version Model Number | A |
Company DUNS | 081334483 |
Company Name | A1 SURGICAL SUPPLIES, LLC |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860000082808 [Primary] |
GS1 | 50860000082803 [Package] Contains: 00860000082808 Package: [50 Units] In Commercial Distribution |
BYY | Tube, Aspirating, Flexible, Connecting |
Steralize Prior To Use | true |
Device Is Sterile | true |
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
[50860000082803]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2018-09-21 |
50860000082810 | Suction tube |
50800000828018 | A |
50860000082803 | A |