Primary Device ID | 05430000620024 |
NIH Device Record Key | 3506a448-4de9-492d-94e3-963ecb6588d5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AT-Adapt |
Version Model Number | ADA010 |
Catalog Number | ADA010 |
Company DUNS | 963361170 |
Company Name | YUKON MEDICAL, LLC |
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 | false |
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 |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Lumen/Inner Diameter | 20 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05430000620017 [Primary] |
GS1 | 05430000620024 [Package] Contains: 05430000620017 Package: Case [100 Units] In Commercial Distribution |
LHI | Set, I.V. Fluid Transfer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-04-30 |
Device Publish Date | 2018-03-29 |
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