Primary Device ID | 10653160306993 |
NIH Device Record Key | 447f0a1f-67d3-4ee4-b047-463b1da46a96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Centurion |
Version Model Number | CSHLDLK2NST R01 |
Company DUNS | 017246562 |
Company Name | CENTURION MEDICAL PRODUCTS CORPORATION |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 | 00653160306996 [Package] Contains: 20653160306990 Package: BOX [10 Units] In Commercial Distribution |
GS1 | 10653160306993 [Package] Contains: 20653160306990 Package: CASE [100 Units] In Commercial Distribution |
GS1 | 20653160306990 [Primary] |
OFD | Catheter introducer 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 | 2018-10-29 |
Device Publish Date | 2017-01-16 |