Primary Device ID | 00810006683318 |
NIH Device Record Key | 13b0ea65-0525-4ba0-85a1-f933374d086d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Preventive Pad |
Version Model Number | PPWD281645 |
Catalog Number | PPWD281645 |
Company DUNS | 958758146 |
Company Name | PRIMO INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 |
---|---|
GS1 | 00810006682151 [Primary] |
GS1 | 00810006683318 [Package] Contains: 00810006682151 Package: Case [10 Units] In Commercial Distribution |
FMP | Protector, Skin Pressure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-30 |
Device Publish Date | 2021-07-22 |
00810006683301 | Preventive Pad - Short (28" x 14" x 4.5") - Wipe Down |
00810006683295 | Preventive Pad - Short (28" x 14" x 4.5") - Sheepskin |
00810006683288 | Preventive Pad - Short (28" x 14" x 4.5") |
00810006680973 | Preventive Pad - Standard (28" x 16" x 4.5") - Wipe Down |
00810006680966 | Preventive Pad - Standard (28" x 16" x 4.5") |
10810006683643 | Preventive Pad - (38" x 14" x 4.5") - Wipe Down |
10810006683629 | Preventive Pad - (38" x 16" x 4.5") - Wipe Down |
00810006683318 | Preventive Pad - (28" x 16" x 4.5") - Wipe Down |