| Primary Device ID | B234KMHRHPRO111115V0 |
| NIH Device Record Key | 5fb5dc22-d989-46df-9f80-c20dd8cf5136 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RH-Pro11 |
| Version Model Number | RH-Pro11 |
| Company DUNS | 601985976 |
| Company Name | CPAC EQUIPMENT, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| 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 |
|---|---|
| HIBCC | B234KMHRHPRO111115V0 [Primary] |
| KMH | Sterilizer, Dry Heat |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-18 |
| Device Publish Date | 2019-01-18 |
| B234KMHRHPRO111230V1 - RH-Pro11-230V | 2020-10-09 High Velocity Hot Air Sterilizer - 230V |
| B234KMHRHPRO9115V3 - RH-Pro9 | 2020-10-09 High Velocity Hot Air Sterilizer - 115V |
| B234KMHRHPRO9115V4 - RH-Pro9-230V | 2020-10-09 High Velocity Hot Air Sterilizer - 230V |
| B234FRGSTMS400633 - STERIDENT | 2020-04-13 Spore Test Monitoring Service Dry Heat or Steam, Mail-in 12/box |
| B234FRGSTMS400634 - STERIDENT | 2020-04-13 SPORE TEST KIT MONITORING SERVICE DRY HEAT OR STEAM, MAIL IN 52/BOX |
| B234FRGDHSB400597 - STERISURE | 2019-11-08 STERISURE DRY HEAT STERILIZER BAGS, PAPER 2.5" X 1.5" X 10.5", 250/BOX |
| B234FRGSSNP400636 - STERIDENT | 2019-11-08 Self-Seal Nylon Pouches 2" x 10" 100/Box |
| B234FRGSSNP400637 - STERIDENT | 2019-11-08 Self-Seal Nylon Pouches 4" x 10" 100/Box |