Primary Device ID | 20886333007855 |
NIH Device Record Key | fdd1259a-6b50-4ffa-8cbf-cb7d6c91faaa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bone Marrow Tray |
Version Model Number | BMT1000 |
Catalog Number | BMT1000 |
Company DUNS | 140727624 |
Company Name | ARGON MEDICAL DEVICES, INC. |
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 | 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com | |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886333007851 [Primary] |
GS1 | 20886333007855 [Package] Contains: 00886333007851 Package: Box [5 Units] In Commercial Distribution |
KNW | Instrument, Biopsy |
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 | 2016-09-20 |
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