Primary Device ID | M209195120 |
NIH Device Record Key | 1a8ffa39-79e6-43aa-bdbe-544ea4c1c64b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Staple Positioner 10x8 |
Version Model Number | 19512 |
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 | M209195120 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | true |
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
[M209195120]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-09 |
Device Publish Date | 2019-05-01 |
M209195120 | 19512 |
00810012484121 | 19512 |