Primary Device ID | 00840828192651 |
NIH Device Record Key | d5421c5c-d91c-4a0f-89f0-c7b8d9f181a3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REGO HUB,ASCOM NU,4FT NC,6FT P |
Version Model Number | HB01-43000001046 |
Catalog Number | 29144 |
Company DUNS | 796452311 |
Company Name | CURBELL MEDICAL PRODUCTS, 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 | 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 |
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00840828192699 - REGO HUB,ASCOM TELLIGENCE,NO-NC,NO-P | 2024-07-30 REGO HUB,ASCOM TELLIGENCE,NO-NC,NO-P |
00840828192705 - REGO HUB,ASCOM NU,9FT-NO-PWR,RELAYS | 2024-07-30 REGO HUB,ASCOM NU,9FT-NO-PWR,RELAYS |
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 |