Primary Device ID | 20884450170292 |
NIH Device Record Key | 81eb72e9-249d-4f88-ac10-3a0b62c0ea3b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flex-Neck® |
Version Model Number | 00884450170298 |
Catalog Number | CF-5242/A |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, 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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450170298 [Primary] |
GS1 | 10884450170295 [Package] Contains: 00884450170298 Package: [1 Units] In Commercial Distribution |
GS1 | 20884450170292 [Package] Contains: 10884450170295 Package: [30 Units] In Commercial Distribution |
FJS | CATHETER, PERITONEAL, LONG-TERM INDWELLING |
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 | 2015-10-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLEX-NECK 78154991 2729292 Live/Registered |
MERIT MEDICAL SYSTEMS, INC. 2002-08-16 |
FLEX-NECK 73698519 1503041 Dead/Cancelled |
MARPAC INDUSTRIES, INC. 1987-12-02 |
FLEX-NECK 73653418 not registered Dead/Abandoned |
MARPAC INDUSTRIES, INC. 1987-04-06 |