RD180® - THE RUNNING DEVICE®
GUDID 10850200006206
RD180® SP™ - THE RUNNING DEVICE® Base Package Type - Each Each sterile package contains (1) single patient use disposable RD180® SP™ (Single Port) Suturing Device.
LSI Solutions, Inc.
Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use| Primary Device ID | 10850200006206 |
| NIH Device Record Key | d857b77b-3f82-49e4-9f5e-4212bbdc39c3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RD180® - THE RUNNING DEVICE® |
| Version Model Number | 021450 |
| Company DUNS | 603420183 |
| Company Name | LSI Solutions, 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 |
Customer Support Contacts
Device Dimensions
| Outer Diameter | 6.4 Millimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Outer Diameter | 6.4 Millimeter |
| Length | 43 Centimeter |
| Length | 43 Centimeter |
| Length | 43 Centimeter |
| Length | 43 Centimeter |
| Length | 43 Centimeter |
| Length | 43 Centimeter |
| Length | 43 Centimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850200006209 [Primary] |
| GS1 | 10850200006206 [Package] Contains: 00850200006209 Package: Case [6 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K100593
FDA Product Code
| HCF | Instrument, Ligature Passing And Knot Tying |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-02-06 |
| Device Publish Date | 2016-09-23 |
On-Brand Devices [RD180® - THE RUNNING DEVICE®]
| 10850200006206 | RD180® SP™ - THE RUNNING DEVICE® Base Package Type - Each Each sterile package contains (1) |
| 10850200006152 | 10 mm RD180® - THE RUNNING DEVICE® Base Package Type - Each Each sterile package contains (1) |
| 10850200006138 | 5 mm RD180® - THE RUNNING DEVICE® Base Package Type - Each Each sterile package contains (1) s |
Trademark Results [RD180]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RD180 85342657 4080216 Live/Registered |
LSI SOLUTIONS, INC. 2011-06-09 |
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