Primary Device ID | B3092G1 |
NIH Device Record Key | 4f48c22f-7540-4556-adb0-afe29ed08f29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Post Medical, Inc. |
Version Model Number | 2G |
Company DUNS | 968012943 |
Company Name | POST MEDICAL, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B3092G0 [Primary] |
HIBCC | B3092G1 [Package] Contains: B3092G0 Package: Case [8 Units] In Commercial Distribution |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-25 |
B309WD200Y1 | WD200Y |
B309WD2000 | WD-200 |
B309WD1501 | WD-150 |
B309WD1101 | WD-110 |
B309SL2001 | SL-200 |
B309SL1501 | SL-150 |
B309SL1001 | SL-100 |
B309PMSM9501 | PMSM-950 |
B3093G1 | 3G |
B3093301LPR1 | 3301-LPR |
B3092GY1 | 2GY |
B3092G1 | 2G |
B3092201LPR1 | 2201-LPR |
B3092201LPBWY1 | 2201-LPBW-Y |
B3092201LPBW1 | 2201-LPBW |
B3091G1 | 1G |
B3091101LPR0 | 1101LPR |
B3091101LPBW0 | 1101-LPBW |