Primary Device ID | 50382903817202 |
NIH Device Record Key | 37fa8169-3fe9-4e50-b816-a1de5970847c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Angiocath-N Autoguard |
Version Model Number | 381720 |
Catalog Number | 381720 |
Company DUNS | 124987988 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 50 |
DM Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382903817207 [Unit of Use] |
GS1 | 30382903817208 [Primary] |
GS1 | 50382903817202 [Package] Contains: 30382903817208 Package: Case [4 Units] In Commercial Distribution |
FOZ | Catheter,intravascular,therapeutic,short-term less than 30 days |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-16 |
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