Primary Device ID | 00887761995055 |
NIH Device Record Key | c70b7e4e-6ed2-484f-b4e9-ae3bfe2b4983 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bassinet |
Version Model Number | P247F |
Company DUNS | 004245668 |
Company Name | HILL-ROM, 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 | 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 |
Phone | +1(800)445-3730 |
us.customerservice@hill-rom.com | |
Phone | +1(800)445-3730 |
us.customerservice@hill-rom.com | |
Phone | +1(800)445-3730 |
us.customerservice@hill-rom.com | |
Phone | +1(800)445-3730 |
us.customerservice@hill-rom.com | |
Phone | +1(800)445-3730 |
us.customerservice@hill-rom.com | |
Phone | +1(800)445-3730 |
us.customerservice@hill-rom.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887761995055 [Primary] |
NZG | Bassinet, hospital |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-17 |
Device Publish Date | 2019-07-09 |
00887761995055 | Bassinet |
00887761996922 | Bassinet |
00887761996915 | Bassinet Surface |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BASSINET 76217710 2757975 Dead/Cancelled |
SANFORD NORTH 2001-03-01 |