Kolibri RMA212
GUDID 05701780272155
Coloplast A/S
Urological surgical procedure kit, non-medicated, single-use| Primary Device ID | 05701780272155 |
| NIH Device Record Key | b79344f5-8430-41f2-a38d-76cdbdbf5be9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kolibri |
| Version Model Number | RMA212 |
| Catalog Number | RMA212 |
| Company DUNS | 305524696 |
| Company Name | Coloplast A/S |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 |
Customer Support Contacts
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com |
Device Dimensions
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
| Catheter Gauge | 12 French |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05701780272148 [Primary] |
| GS1 | 05701780272155 [Package] Contains: 05701780272148 Package: Retail Box [1 Units] In Commercial Distribution |
| GS1 | 05701780272162 [Package] Package: Shipper Box [24 Units] In Commercial Distribution |
FDA Product Code
| LJE | CATHETER, NEPHROSTOMY |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-10-07 |
| Device Publish Date | 2023-01-20 |
On-Brand Devices [Kolibri]
| 05701780272186 | RMA214 |
| 05701780272155 | RMA212 |
| 05701780272131 | RMA210 |
| 05701780272100 | RMA208 |
| 05701780272063 | RMA114 |
| 05701780272049 | RMA112 |
| 05701780272001 | RMA110 |
| 05701780271974 | RMA108 |
| 05701780271950 | RJB210 |
| 05701780271912 | RJB208 |
| 05701780271875 | RJB110 |
| 05701780271851 | RJB109 |
| 05701780271813 | RJB108 |
| 05701780271783 | RJB007 |
| 05701780271745 | RJB006 |
| 05701780271714 | RJA212 |
| 05701780271677 | RJA210 |
| 05701780271646 | RJA208 |
| 05701780271622 | RJA114 |
| 05701780271592 | RJA112 |
| 05701780271547 | RJA110 |
| 05701780271509 | RJA108 |
| 05701780271462 | RJA008 |
| 05701780271448 | RJA006 |
| 05701780271417 | RCM014 |
| 05701780271363 | RCM012 |
| 05701780271332 | RCM010 |
| 05701780271318 | RCM008 |
| 05701780271271 | RCJ114 |
| 05701780271240 | RCJ112 |
| 05701780271219 | RCJ110 |
| 05701780271189 | RCJ109 |
| 05701780271165 | RCJ108 |
| 05701780271127 | RCJ008 |
| 05701780271097 | RCJ007 |
| 05701780271066 | RCJ006 |
| 05701780271042 | RJD110 |
| 05701780270977 | RJD108 |
| 05701780270939 | RCM020 |
| 05701780270908 | RCM018 |
| 05701780270878 | RCM016 |
Trademark Results [Kolibri]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KOLIBRI 87842075 5712417 Live/Registered |
KOLIBRI DRINKS LIMITED 2018-03-20 |
 KOLIBRI 87708177 5891917 Live/Registered |
TEKSTRA BRANDS INC. 2017-12-05 |
 KOLIBRI 87584427 5463018 Live/Registered |
Cassida Corporation 2017-08-25 |
 KOLIBRI 87181671 5314952 Live/Registered |
Foundation for Learning Equality, Inc. 2016-09-23 |
 KOLIBRI 87061250 not registered Dead/Abandoned |
Everest Partners, LLC 2016-06-06 |
 KOLIBRI 87027518 not registered Dead/Abandoned |
Roman Zavolunov 2016-05-06 |
 KOLIBRI 86915279 not registered Dead/Abandoned |
Laura Reddy, a U.S. citizen and Paul Pinthon, a citizen of France, Trustees of Aravinda Trust 2016-02-22 |
 KOLIBRI 86839623 not registered Live/Pending |
TEKSTRA BRANDS INC. 2015-12-04 |
 KOLIBRI 80954917 0954917 Dead/Cancelled |
Lehmann; Dieter 0000-00-00 |
 KOLIBRI 79197305 5682505 Live/Registered |
INTERNATIONAL TECHNOLOGY CENTER FZC 2016-04-21 |
 KOLIBRI 79131095 not registered Dead/Abandoned |
Society With Limited Liability; "Kolibri" 2013-03-18 |
 KOLIBRI 79122662 4690253 Live/Registered |
Coloplast A/S 2012-11-29 |
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