Primary Device ID | 05060548020453 |
NIH Device Record Key | f84b2c23-6e3d-4a63-bf9d-1ff2b5d48937 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Apex ASG |
Version Model Number | 965-1205 |
Catalog Number | 965-1205 |
Company DUNS | 222236587 |
Company Name | BIOSTONE CO. LIMITED |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060548020453 [Primary] |
MQV | Filler, Bone Void, Calcium Compound |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-13 |
Device Publish Date | 2025-02-05 |
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