Primary Device ID | 00815137021114 |
NIH Device Record Key | 8b40ae7a-ebc9-4fa7-8240-09b16816d59d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GuideLines |
Version Model Number | 217 |
Company DUNS | 001157841 |
Company Name | Beekley Corporation |
Device Count | 15 |
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 | false |
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 | 00815137021114 [Primary] |
GS1 | 10815137021111 [Unit of Use] |
IXJ | Grid, Radiographic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-30 |
Device Publish Date | 2019-07-22 |
00815137021558 | CT Grid for Localizing Needle Entry Sites, 7x7.5" biopsy grid |
00815137021510 | CT Grid for Localizing Needle Entry Sites, 4x5" biopsy grid |
00815137021114 | CT Grid for Localizing Needle Entry Sites, 7x7.5" biopsy grid |
00815137020063 | CT Grid for Localizing Needle Entry Sites, 4x5" biopsy grid |