Primary Device ID | 20886333227116 |
NIH Device Record Key | 0081b1fb-0386-4c0b-be9e-4dead25936c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bone Access Needle |
Version Model Number | DBANJ0806TL |
Catalog Number | DBANJ0806TL |
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 | 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 | true |
OTC Over-The-Counter | false |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com | |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com | |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry and away from sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry and away from sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry and away from sunlight |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886333227112 [Primary] |
GS1 | 20886333227116 [Package] Contains: 00886333227112 Package: Box [10 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 | 2025-01-23 |
Device Publish Date | 2023-01-03 |
20886333223200 | Bone Access Needle 11ga x 6in |
20886333222951 | Bone Access Needle 11ga x 4in |
20886333222944 | Bone Access Needle 11ga x 4in |
20886333227116 | Bone Access Needle 8ga x 6in |