Primary Device ID | 50628725098017 |
NIH Device Record Key | 89f252f1-cfdf-4795-82ee-25feec20d708 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Swivel Tubing Connector |
Version Model Number | R-3000 |
Catalog Number | R-3000 |
Company DUNS | 243175213 |
Company Name | Respan Products Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00628725098012 [Primary] |
GS1 | 50628725098017 [Package] Contains: 00628725098012 Package: Corrugate Case [10 Units] In Commercial Distribution |
CAT | Cannula, Nasal, Oxygen |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-22 |
Device Publish Date | 2023-06-14 |
50628725098017 | CONNECTOR SWIVEL MALE TO MALE |
50628725097607 | CONNECTOR SWIVEL TUBING MALE TO MALE |
50628725097379 | CONNECTOR SWIVEL TUBING FEMALE TO MALE |