Primary Device ID | 10653160235088 |
NIH Device Record Key | 9ec24e05-5855-4bf7-8c0f-36927812140c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Centurion |
Version Model Number | DC4065ST |
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 | 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 | 00653160235081 [Primary] |
GS1 | 10653160235088 [Package] Contains: 00653160235081 Package: CASE [28 Units] In Commercial Distribution |
KKX | Drape, surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-11-08 |
Device Publish Date | 2016-09-07 |