Primary Device ID | 07540161750015 |
NIH Device Record Key | 6b88e150-db14-42a5-99ac-f491c9311ca7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AbClo |
Version Model Number | ABCLO001 |
Company DUNS | 204358506 |
Company Name | Inventorr MD Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07540161750015 [Primary] |
MKY | System, Skin Closure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-12 |
Device Publish Date | 2023-12-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ABCLO 97040363 not registered Live/Pending |
InventoRR MD Inc. 2021-09-22 |