Flex-Neck® CF-5460
GUDID 10884450727840
Merit Medical Systems, Inc.
Peritoneal dialysis catheter, chronic| Primary Device ID | 10884450727840 |
| NIH Device Record Key | e2aa27e5-1383-4938-b8f5-b40969fd0ae4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Flex-Neck® |
| Version Model Number | D |
| Catalog Number | CF-5460 |
| 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 | true |
| OTC Over-The-Counter | false |
Device Dimensions
| Device Size Text, specify | 0 |
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Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450727843 [Primary] |
| GS1 | 10884450727840 [Package] Contains: 00884450727843 Package: [30 Units] In Commercial Distribution |
FDA Product Code
| FJS | Catheter, peritoneal, long-term indwelling |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-14 |
| Device Publish Date | 2024-06-06 |
On-Brand Devices [Flex-Neck®]
Trademark Results [Flex-Neck]
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 |
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