Primary Device ID | 00616784492537 |
NIH Device Record Key | 70e49ab9-5bed-4736-b6ba-82c7174472b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Urethral Catheterization Tray |
Version Model Number | 4925 |
Company DUNS | 008124539 |
Company Name | DYNAREX 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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00616784492520 [Primary] |
GS1 | 00616784492537 [Package] Contains: 00616784492520 Package: [20 Units] In Commercial Distribution |
FCM | Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-04-09 |
Device Publish Date | 2016-09-24 |
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