| Primary Device ID | 10866305000247 |
| NIH Device Record Key | f1996f12-7332-4bd5-96ec-37a24ac69f89 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RapidWeld Blade Module Kit |
| Version Model Number | GRW-430 |
| Catalog Number | 480-RW-2478-02 |
| Company DUNS | 141091095 |
| Company Name | GENESIS BPS LLC |
| Device Count | 500 |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | true |
| Phone | 201-708-1400 |
| info@genesisbps.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00866305000240 [Unit of Use] |
| GS1 | 10866305000247 [Primary] |
| KSB | Set, Transfer (Blood/Plasma) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-20 |
| Device Publish Date | 2020-01-10 |
| 10866305000254 | The Blade Module consists of a stainless steel blade that cuts the PVC tube segments. The Blade |
| 10866305000247 | The Blade Module consists of a stainless steel blade that cuts the PVC tube segments. The Blade |
| 10866305000230 | The Blade Module consists of a stainless steel blade that cuts the PVC tube segments. The Blade |