| Primary Device ID | 04046964941115 |
| NIH Device Record Key | a3f3d7af-c825-4f69-ab7e-50fcd6fb4731 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PERIFIX™ |
| Version Model Number | 339163 |
| Catalog Number | 339163 |
| Company DUNS | 002397347 |
| Company Name | B. BRAUN MEDICAL INC. |
| Device Count | 50 |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
| Phone | +1(800)227-2862 |
| BBMUS_Service.EmailOrders@bbraun.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04046964941108 [Unit of Use] |
| GS1 | 04046964941115 [Primary] |
| CAZ | Anesthesia conduction kit |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-03-03 |
| Device Publish Date | 2016-11-06 |
| 04046964941139 | PCC2000N 20GA - 24GA CATH CONN NRFIT |
| 04046964941115 | PCC1900N 19GA CATH CONN NRFIT |
| 04046955735471 | PERIFIX 10 ML GLASS LOR SYR LOCK NRFIT |
| 04046955735457 | PERIFIX 10 ML GLASS LOR SYR SLIP NRFIT |
| 04046955768233 | 18GA X 4.75 TOUHY NEEDLE EPIDURAL-NRFIT |
| 04046964941054 | FEF100N FLAT EPIDURAL FILTER NRFIT |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PERIFIX 73696327 1713357 Live/Registered |
B. BRAUN MELSUNGEN AKTIENGESELLSCHAFT 1987-11-19 |