Primary Device ID | 00887761999114 |
NIH Device Record Key | 56bd0e97-f3bc-4b62-958a-679f91b1ed25 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Centrella™ Surface |
Version Model Number | P7920A |
Company DUNS | 004245668 |
Company Name | HILL-ROM, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 | 00887761999114 [Primary] |
IKY | MATTRESS, FLOTATION THERAPY, NON-POWERED |
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 | 2017-06-29 |
00887761999114 | Hospital Bed Surface |
00887761999107 | Hospital Bed Surface |
00887761999091 | Hospital Bed Surface |
00887761999084 | Hospital Bed Surface |
00887761999077 | Hospital Bed Surface |
00887761984639 | Hospital Bed Surface |
00887761976979 | Hospital Bed Surface |
00887761976962 | Hospital Bed Surface |
00887761966819 | Centrella Air, Replacement, X-Ray, sleeve, Top Cover |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CENTRELLA 87407023 5466008 Live/Registered |
Hill-Rom Services, Inc. 2017-04-11 |
CENTRELLA 87357966 5465798 Live/Registered |
Hill-Rom Services, Inc. 2017-03-03 |
CENTRELLA 73143214 1106500 Dead/Expired |
CENTRAL GROCERS COOPERATIVE, INC. 1977-09-30 |