Primary Device ID | 00815137021961 |
NIH Device Record Key | e2e2d7a2-3438-4ac0-b049-0ffc65f5739f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MarginMap |
Version Model Number | 308S |
Company DUNS | 001157841 |
Company Name | Beekley Corporation |
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 | 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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815137021961 [Primary] |
MJI | Specimen/Tissue, Identification Orientation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-30 |
Device Publish Date | 2019-07-22 |
00815137021961 | Specimen Orientation Charms, six distinctly shaped sterile 10mm charms |
00815137021954 | Specimen Orientation Charms, six distinctly shaped sterile 5mm charms |
00815137020216 | Specimen Orientation Charms, six distinctly shaped sterile 10mm charms |
00815137020209 | Specimen Orientation Charms, six distinctly shaped sterile 5mm charms |