Primary Device ID | 00850391007214 |
NIH Device Record Key | f43524da-f212-48c0-93f6-c427181ce65b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Montage Flowable Tips (3x) |
Version Model Number | 900-MFL |
Company DUNS | 078818942 |
Company Name | ABYRX, INC. |
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 | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850391007214 [Primary] |
MTJ | Wax, Bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-17 |
Device Publish Date | 2021-03-09 |
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