Primary Device ID | 00616784705637 |
NIH Device Record Key | 0e51f54e-be2b-4c6e-8cdd-5afbec8baed2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Needless PRN Pre-Pierced Port Converter |
Version Model Number | 7056 |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 00616784705613 [Primary] |
GS1 | 00616784705637 [Package] Contains: 00616784705613 Package: Case [100 Units] In Commercial Distribution |
GS1 | 00616784705644 [Package] Package: Shipper [4 Units] In Commercial Distribution |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-23 |
Device Publish Date | 2021-09-15 |
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