Primary Device ID | B234KMHRHPRO9115V3 |
NIH Device Record Key | 41a5e3e6-7d4c-4e39-83b4-03735186715c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RH-Pro9 |
Version Model Number | RH-Pro9 |
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 | 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 |
---|---|
HIBCC | B234KMHRHPRO9115V3 [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 | 2020-10-09 |
Device Publish Date | 2020-10-01 |
B234KMHRHPRO111230V1 - RH-Pro11-230V | 2020-10-09 High Velocity Hot Air Sterilizer - 230V |
B234KMHRHPRO9115V3 - RH-Pro9 | 2020-10-09High Velocity Hot Air Sterilizer - 115V |
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 |