Primary Device ID | 10841912100504 |
NIH Device Record Key | 32863854-f7fe-4f45-accc-0ec97e703a83 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CT Control Cover |
Version Model Number | 1006 |
Catalog Number | 1006 |
Company DUNS | 965417181 |
Company Name | PROTEK MEDICAL PRODUCTS, INC. |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841912100507 [Primary] |
GS1 | 10841912100504 [Package] Contains: 00841912100507 Package: [50 Units] In Commercial Distribution |
KKX | Drape, Surgical |
MMP | Cover, Barrier, Protective |
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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