Primary Device ID | 08809255542707 |
NIH Device Record Key | b96a2d2b-a648-4d75-9702-ef3ce55c7a63 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GUARDIAN Inflatable Bone Expander System |
Version Model Number | BMK15-1 |
Company DUNS | 557799209 |
Company Name | BM KOREA CO., LTD |
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 | true |
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 |
Length | 303 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809255542707 [Primary] |
HRX | Arthroscope |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2018-02-14 |
08809255544817 | The GUARDIAN Inflatable Bone Expander System is designed to reduce spinal compression fracture a |
08809255542707 | The GUARDIAN Inflatable Bone Expander System is designed to reduce spinal compression fracture a |
08809255544213 | The GUARDIAN Inflatable Bone Expander System is designed to reduce spinal compression fracture a |
08809255544169 | The GUARDIAN Inflatable Bone Expander System is designed to reduce spinal compression fracture a |