Primary Device ID | 05030267006625 |
NIH Device Record Key | 1691af0c-4ba9-4536-9073-c7988d23c07e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FIXED ELBOW 22F - 6MM STEM - 22M |
Version Model Number | 1991000 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05030267006625 [Package] Contains: 05030267057986 Package: [20 Units] In Commercial Distribution |
GS1 | 05030267006632 [Package] Contains: 05030267057986 Package: [80 Units] In Commercial Distribution |
GS1 | 05030267057986 [Primary] |
BZA | Connector, Airway (Extension) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-23 |
Device Publish Date | 2023-06-15 |