| Primary Device ID | 00887761976726 |
| NIH Device Record Key | c8566705-1bca-41f5-8d43-7e51223714ed |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Proning Accessory Kit |
| Version Model Number | P7529 |
| 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 | 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 | 00887761976726 [Primary] |
| FNL | BED, AC-POWERED ADJUSTABLE 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 | 2021-06-08 |
| Device Publish Date | 2021-05-31 |
| 00887761976542 - Experience Pod | 2025-01-28 Experience Pod |
| 00887761007710 - Centrella™ Surface | 2024-12-05 CENTRELLA® MAX SURFACE |
| 00887761007727 - Centrella™ Surface | 2024-12-05 CENTRELLA® MAX SURFACE WITH X-RAY |
| 00887761007734 - Centrella™ Surface | 2024-12-05 CENTRELLA® MAX SURFACE |
| 00887761007741 - Centrella™ Surface | 2024-12-05 CENTRELLA® MAX, NARROW, RENTAL |
| 00887761007758 - Centrella™ Surface | 2024-12-05 CENTRELLA® MAX, WIDE, RENTAL |
| 00887761007765 - Centrella™ Surface | 2024-12-05 CENTRELLA AIR, REPLACEMENT, X-RAY SLEEVE, TOP COVER |
| 00887761966819 - Centrella™ Surface | 2024-09-30 Centrella Air, Replacement, X-Ray, sleeve, Top Cover |