| Primary Device ID | M209183000 |
| NIH Device Record Key | 69c9cf84-8d29-4d3f-8502-eb780551c69b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pusher 4 leg 14x12 |
| Version Model Number | 18300 |
| 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 | M209183000 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
Moist Heat or Steam Sterilization
[M209183000]
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 |
| M209183000 | 18300 |
| 00810012483971 | 18300 |