Primary Device ID | 20886333208573 |
NIH Device Record Key | 962bf118-68f5-463c-9d16-a61852dc1c42 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Manifold Kit |
Version Model Number | 196033 |
Catalog Number | 196033 |
Company DUNS | 140727624 |
Company Name | ARGON MEDICAL DEVICES, INC. |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886333208579 [Primary] |
GS1 | 20886333208573 [Package] Contains: 00886333208579 Package: Box [10 Units] In Commercial Distribution |
OJA | Intravenous Extension Tubing Set |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-21 |
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