| Primary Device ID | 16972620112351 |
| NIH Device Record Key | b591a867-ee94-4655-beee-35a241adb373 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Right Way Medical |
| Version Model Number | RWM-IFRF01 |
| Company DUNS | 544463583 |
| Company Name | BQ PLUS MEDICAL CO., LTD. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 16972620112351 [Primary] |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
[16972620112351]
Ethylene Oxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-31 |
| Device Publish Date | 2025-03-21 |
| 26972620112358 | RWM-IFRF01 |
| 16972620112351 | RWM-IFRF01 |
| 06972620112347 | RWM-IFRF01 |