Primary Device ID | 36704820000022 |
NIH Device Record Key | 738a5f81-27ab-4c1a-88f7-a84292ed26ac |
Commercial Distribution Discontinuation | 2016-09-21 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | MedSurg Manual Bed |
Version Model Number | FL23P |
Catalog Number | FL23P |
Company DUNS | 249675476 |
Company Name | Umano Medical 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 | true |
Manufacturing Date | true |
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 | 16704820000028 [Primary] |
GS1 | 26704820000025 [Package] Contains: 16704820000028 Package: [1 Units] Discontinued: 2016-09-21 Not in Commercial Distribution |
GS1 | 36704820000022 [Package] Contains: 16704820000028 Package: [2 Units] Discontinued: 2016-09-21 Not in Commercial Distribution |
FNJ | Bed, Manual |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-11-30 |
00670482000029 | MedSurg Manual Bed |
36704820000022 | MedSurg Manual Bed |