Rapid Rhino
- Primary DI
- 20817470000508
- Brand
- Rapid Rhino
- Company
- Smith & Nephew, Inc.
- Model
- RR 900
- Catalog number
- RR 900
- Device description
- 9CM ANTERIOR/POSTERIOR DUAL
- Published
- 2015-08-29
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| EMX | BALLOON, EPISTAXIS |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| EMX | Balloon, Epistaxis | Ear, Nose, Throat | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20817470000508 | Package | GS1 | 10 | In Commercial Distribution |
| 00817470000504 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20817470000508 | 20817470000508 | ||
| 00817470000504 | 00817470000504 | 817470000504 | 0817470000504 |
GMDN Terms#
| Term | Definition |
|---|---|
| Epistaxsis balloon | A device consisting of a hollow rubber or rubber-like structure, expandable with either liquid or air, intended to be used to control nose bleeding (epistaxis) of the anterior or posterior nasal cavity. It is applied during an ear/nose/throat (ENT) intervention and can also be used to treat glue ear in children, and/or to support the structure and patency of the nasal canal. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 109903521
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 03596010482280 | CLEAR-TRAC | 7210121 | 7210121 | 2015-10-22 |
| 03596010532619 | NA | 7210719 | 7210719 | 2015-08-30 |
| 03596010505132 | SCULPTOR | 7210697 | 7210697 | 2015-08-30 |
| 03596010505149 | SCULPTOR | 7210696 | 7210696 | 2015-08-30 |
| 03596010505170 | SCULPTOR | 7210695 | 7210695 | 2015-08-30 |
| 03596010505194 | SCULPTOR | 7210700 | 7210700 | 2015-08-30 |
| 00885554016703 | 560P | 72202351 | 72202351 | 2015-08-29 |
| 00885556919781 | Real Intelligence | ROB30007 | ROB30007 | 2026-10-13 |
| 00885556924327 | Real Intelligence | ROB30801 | ROB30801 | 2026-10-08 |
| 03596010445803 | NA | 7209030 | 7209030 | 2015-08-30 |
| 03596010470294 | SAPHYRE | 7209684 | 7209684 | 2015-08-30 |
| 03596010470331 | ABLATOR | 7209659 | 7209659 | 2015-08-30 |
| 03596010470348 | ABLATOR | 7209658 | 7209658 | 2015-08-30 |
| 03596010470416 | ABLATOR | 7209651 | 7209651 | 2015-08-30 |
| 03596010470577 | ABLATOR | 7209650 | 7209650 | 2015-08-30 |
| 03596010470614 | TAC-S | 7209632 | 7209632 | 2015-08-30 |
| 03596010448446 | TWINFIX | 7209109 | 7209109 | 2015-08-30 |
| 03596010470393 | ABLATOR | 7209653 | 7209653 | 2015-08-30 |
| 03596010470423 | ABLATOR | 7209649 | 7209649 | 2015-08-30 |
| 03596010510976 | NA | 7210040 | 7210040 | 2015-08-30 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00821925034662 | Gyrus ACMI | Gyrus ACMI, LLC | EMX | 2024-11-26 |
| 00821925042391 | Gyrus ACMI | Gyrus ACMI, LLC | EMX | 2024-07-25 |
| 08904428722075 | OSSEOUS | EON MEDITECH PRIVATE LIMITED | EMX | 2024-06-11 |
| 08904428722082 | OSSEOUS | EON MEDITECH PRIVATE LIMITED | EMX | 2024-06-11 |
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