Primary Device ID | M209122370 |
NIH Device Record Key | a33330ef-543f-4d91-b0bf-f799c8935c97 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MPJ Trial 23mm (LG) |
Version Model Number | 12237 |
Company DUNS | 618749857 |
Company Name | BIOPRO, 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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M209122370 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
[M209122370]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-04-06 |
Device Publish Date | 2019-05-02 |
M209122370 | 12237 |
00810012485371 | 12237 |