Primary Device ID | 38498840010533 |
NIH Device Record Key | 38697e72-c36f-4770-b86c-673d9f8d0713 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Churchill Medical Systems |
Version Model Number | BHS-2250 |
Catalog Number | BHS-2250 |
Company DUNS | 120818216 |
Company Name | Vygon Corporation |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 |
---|---|
GS1 | 08498840010532 [Primary] |
GS1 | 38498840010533 [Package] Contains: 08498840010532 Package: [12 Units] In Commercial Distribution |
FPA | Set, administration, intravascular |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2019-05-20 |
38498840010540 | 10" WINGED SAFETY INFUSION SET W/22 GA. X .75" HUBER NEEDLE AND NEEDLELESS Y-SITE |
38498840010533 | 10" WINGED SAFETY INFUSION SET W/22 GA. X .5" HUBER NEEDLE |
38498840010526 | 10" WINGED SAFETY INFUSION SET W/22 GA. X .75" HUBER NEEDLE |
38498840010519 | 10" WINGED SAFETY INFUSION SET W/20 GA. X .75" (19MM) HUBER NEEDLE |
38498840010731 | 10" WINGED SAFETY INFUSION SET W/20 GA. X 1.0" HUBER NEEDLE |
38498840010380 | 10" WINGED SAFETY INFUSION SET W/22 GA. X 1.0" HUBER NEEDLE AND NEEDLELESS Y-SITE |
38498840010373 | 10" WINGED SAFETY INFUSION SET W/20 GA. X .75" HUBER NEEDLE AND NEEDLELESS Y-SITE |
38498840010267 | 10" WINGED SAFETY INFUSION SET W/20 GA. X 1.0" HUBER NEEDLE AND NEEDLELESS Y-SITE |