Capella™ MK5183
GUDID 00821329400346
5 French Coaxial Micro-Introducer Kit
Greatbatch Ltd
Vascular catheter introduction set, nonimplantable| Primary Device ID | 00821329400346 |
| NIH Device Record Key | f6b0675c-f495-41b6-a620-a513061c018e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Capella™ |
| Version Model Number | 1012868-006 |
| Catalog Number | MK5183 |
| Company DUNS | 968623467 |
| Company Name | Greatbatch Ltd |
| 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 | 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 Dimensions
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 9.3 Centimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00821329400346 [Primary] |
| GS1 | 10821329400343 [Package] Package: [10 Units] In Commercial Distribution |
FDA Product Code
| DYB | Introducer, Catheter |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-03-06 |
| Device Publish Date | 2016-04-05 |
On-Brand Devices [Capella™]
| 00821329400346 | 5 French Coaxial Micro-Introducer Kit |
| 00821329400339 | 5 French Coaxial Micro-Introducer Kit |
| 10821329400329 | 5 French Coaxial Micro-Introducer Kit |
| 00821329400315 | 4 French Coaxial Micro-Introducer Kit |
| 10821329400305 | 4 French Coaxial Micro-Introducer Kit |
| 00821329400292 | 4 French Coaxial Micro-Introducer Kit |
Trademark Results [Capella]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CAPELLA 98494754 not registered Live/Pending |
Symphony Park Vegas C, LLC 2024-04-11 |
 CAPELLA 98242139 not registered Live/Pending |
LivaNova USA, Inc 2023-10-26 |
 CAPELLA 97553625 not registered Live/Pending |
Tacony Corporation 2022-08-18 |
 CAPELLA 97313270 not registered Live/Pending |
STAR EV Corporation 2022-03-15 |
 CAPELLA 90747262 not registered Live/Pending |
Capella Space Corp. 2021-06-01 |
 CAPELLA 88205239 5804567 Live/Registered |
Capella Flavors, Inc. 2018-11-26 |
 CAPELLA 88134944 not registered Live/Pending |
Spigen Korea Co., Ltd. 2018-09-27 |
 CAPELLA 87841544 5605931 Live/Registered |
DECOY INTERNATIONAL, INC. 2018-03-20 |
 CAPELLA 87841523 not registered Dead/Abandoned |
DECOY INTERNATIONAL, INC. 2018-03-20 |
 CAPELLA 87770088 5541037 Live/Registered |
ECLIPSE.ORG FOUNDATION, INC. 2018-01-25 |
 CAPELLA 87727770 5534345 Live/Registered |
ECLIPSE.ORG FOUNDATION, INC. 2017-12-20 |
 CAPELLA 87501727 not registered Dead/Abandoned |
E & E CO., LTD. 2017-06-22 |
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