Primary Device ID | 00840828188265 |
NIH Device Record Key | 44f99f6f-fb96-4fc8-a638-1b6b67bf6e33 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RLW,PINCH,SAFETY DIN,24",WHT (RA) |
Version Model Number | RLW-01BA-24RA-0000 |
Catalog Number | 28007 |
Company DUNS | 796452311 |
Company Name | CURBELL MEDICAL PRODUCTS, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
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 | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
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00840828192712 - UNDER BED LIGHT CONTROLLER ASSEMBLY | 2024-07-30 UNDER BED LIGHT CONTROLLER ASSEMBLY |
00840828192729 - RESPONDER 5, INTERACTIVE | 2024-07-30 RESPONDER 5, INTERACTIVE |
00840828192736 - GEN4 PLUS, DIRECT ACCESS | 2024-07-30 GEN4 PLUS, DIRECT ACCESS |
00840828192743 - GEN4 INTERACTIVE | 2024-07-30 GEN4 INTERACTIVE |
00840828192750 - GEN4 PLUS, RESPONDER 5, ENHANCED | 2024-07-30 GEN4 PLUS, RESPONDER 5, ENHANCED |