Primary Device ID | 20020221265396 |
NIH Device Record Key | 7d2676d5-cef6-481f-9b30-cc8b050b1ccb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EXEL Injection Plug with Cap |
Version Model Number | 26539 |
Catalog Number | 26539 |
Company DUNS | 180572216 |
Company Name | Exel International |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00020221265392 [Unit of Use] |
GS1 | 10020221265399 [Primary] |
GS1 | 20020221265396 [Package] Contains: 10020221265399 Package: [4 Units] In Commercial Distribution |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2023-11-08 |
Device Publish Date | 2016-09-22 |
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