Primary Device ID | 01816835023393 |
NIH Device Record Key | 5a03dc8b-1683-4c6b-9314-44204cd78736 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NUVO PADS |
Version Model Number | B2DCP001634 |
Company DUNS | 093357739 |
Company Name | MEDICAL ILLUMINATION INTERNATIONAL 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 | false |
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 | 00816835023394 [Primary] |
GS1 | 01816835023393 [Package] Contains: 00816835023394 Package: BOX [1 Units] In Commercial Distribution |
FWZ | Operating Room Accessories Table Tray |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-04-08 |
Device Publish Date | 2020-03-31 |
00816835023530 | Shoulder Attach, Back Pad |
01816835023522 | Shoulder Attach. Side Pad |
01816835023515 | IA Extender Pad |
00816835023509 | Lateral Pelvis Pad |
01816835023492 | Ophthalmic Headrest Pad |
01816835023485 | Narrow Perineal Cutout Pad |
01816835023478 | Wide Perineal Cutout Pad |
01816835023461 | Hour Glass Table Pad |
01816835023454 | Supine Pelvis Pad |
01816835023447 | Wide Supine Pelvis Pad |
01816835023430 | B2DCP001731 |
01816835023423 | Foot Rest Pad |
01816835023416 | Arm Board Pad |
01816835023409 | Split leg Pad, R |
01816835023393 | Split Leg Pad, L |
01816835023386 | Body Section Pad |
01816835023379 | Head Section Pad |
01816835023362 | Body Section Pad |
01816835023355 | Extension Pad |
01816835023348 | Short Leg Pad |