Primary Device ID | 00889024205505 |
NIH Device Record Key | fbb32e14-2dc1-41bb-b78f-8f04fb3def85 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Beta-bsm ® |
Version Model Number | 76-6025 |
Company DUNS | 622221141 |
Company Name | Etex Corporation |
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 | 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 |
Phone | 877-383-9276 |
sales@etexcorp.com |
Total Volume | 2.5 Milliliter |
Special Storage Condition, Specify | Between 0 and 0 *Store at 15-25 Degrees Celcius Keep Dry Keep Away From Sunlight |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024205505 [Primary] |
MQV | Filler, Bone Void, Calcium Compound |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-11 |
Device Publish Date | 2015-10-24 |
00889024205512 | 76-6016 |
00889024205505 | 76-6025 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BETA-BSM 77834551 3990684 Live/Registered |
ETEX CORPORATION 2009-09-24 |