Respan RC710
GUDID 50628725097515
NASAL CANNULA ADULT LARIAT STYLE STRAIGHT TIP KRATON W 7' SAFLO OXYGEN
Respan Products Inc
Nasal oxygen cannula, basic| Primary Device ID | 50628725097515 |
| NIH Device Record Key | 1b56e7cb-0e76-46d7-bb61-e44c4a1a8c8a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Respan |
| Version Model Number | RC710 |
| Catalog Number | RC710 |
| Company DUNS | 243175213 |
| Company Name | Respan Products Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00628725097510 [Primary] |
| GS1 | 50628725097515 [Package] Contains: 00628725097510 Package: Corrugate Case [50 Units] In Commercial Distribution |
FDA Product Code
| CAT | Cannula, Nasal, Oxygen |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-27 |
| Device Publish Date | 2023-06-19 |
On-Brand Devices [Respan]
| 50628725097515 | NASAL CANNULA ADULT LARIAT STYLE STRAIGHT TIP KRATON W 7' SAFLO OXYGEN |
| 50628725097683 | MASK ADULT FILTER OXYGEN NEBULIZER KIT W/ 7' SAFLO OXYGEN |
Trademark Results [Respan]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RESPAN 77843163 3875666 Live/Registered |
Respan Products Inc. 2009-10-07 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.