Primary Device ID | 00815137020285 |
NIH Device Record Key | 6272f808-c54e-4164-9858-ffccfccb4c07 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pinnacle |
Version Model Number | 330 |
Company DUNS | 001157841 |
Company Name | Beekley Corporation |
Device Count | 12 |
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 | 00815137020285 [Primary] |
GS1 | 10815137020282 [Unit of Use] |
KGX | Tape And Bandage, Adhesive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2019-07-22 |
00815137021640 | Needle Localization Needle Protectors |
00815137020285 | Needle Localization Needle Protectors |