POSTERIOR BALLOON CATHETER SILICONE
- Primary DI
- 00821925022195
- Brand
- POSTERIOR BALLOON CATHETER SILICONE
- Company
- Gyrus Acmi, Inc.
- Model
- 890922
- Published
- 2018-09-13
- 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
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 |
|---|---|---|---|---|
| 00821925022195 | Package | GS1 | 6 | In Commercial Distribution |
| 00821925040335 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00821925022195 | 00821925022195 | 821925022195 | 0821925022195 |
| 00821925040335 | 00821925040335 | 821925040335 | 0821925040335 |
GMDN Terms#
| Term | Definition |
|---|---|
| Nasal/paranasal balloon catheter | A sterile flexible tube with an inflatable balloon at its distal tip designed to gently restructure nasal passages and dilate obstructed sinus ostia during a surgical procedure (sinuplasty), typically to treat sinusitis, and/or to gently restructure nasal passages to temporarily relieve nasal obstruction/congestion. The device typically consists of a single-lumen tube with a connector at the proximal end for attachment to an inflation device. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 007198742
- 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 |
|---|---|---|---|---|
| 00821925043916 | SOLTIVE | TFL-FBX150BS | 2024-08-01 | |
| 00821925043930 | SOLTIVE | TFL-FBX200S | 2024-08-01 | |
| 00821925043978 | SOLTIVE | TFL-FBX200BS | 2024-08-01 | |
| 00821925043992 | SOLTIVE | TFL-FBX365S | 2024-08-01 | |
| 00821925044074 | SOLTIVE | TFL-FBX940S | 2024-08-01 | |
| 00821925000933 | Gyrus ACMI | 20714 | 2024-07-25 | |
| 00821925025929 | DIEGO | 70139000 | 2024-07-25 | |
| 00821925025936 | DIEGO | 70139002 | 2024-07-25 | |
| 00821925025974 | DIEGO | 70139010 | 2024-07-25 | |
| 00821925025967 | DIEGO | 70139008 | 2024-07-25 | |
| 00821925000469 | Gyrus ACMI | 005-5-101 | 2024-07-25 | |
| 00821925000476 | Gyrus ACMI | 005-5-201 | 2024-07-25 | |
| 00821925000483 | Gyrus ACMI | 005-5-301 | 2024-07-25 | |
| 00821925000490 | Gyrus ACMI | 005-5-401 | 2024-07-25 | |
| 00821925010932 | Gyrus ACMI | 608BX | 2024-07-25 | |
| 00821925025943 | DIEGO | 70139004 | 2024-07-25 | |
| 00821925022379 | Gyrus ACMI | 890912 | 2024-07-25 | |
| 00821925010819 | Gyrus ACMI | 7035-3006 | 2024-07-25 | |
| 00821925043077 | DIEGO ELITE | BB4000SC | 2024-07-25 | |
| 00821925043879 | SOLTIVE | TFL-FBX150S | 2024-07-25 |
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 |
| 08904428722099 | OSSEOUS | EON MEDITECH PRIVATE LIMITED | EMX | 2024-06-11 |
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| 08904428722341 | OSSEOUS | EON MEDITECH PRIVATE LIMITED | EMX | 2024-06-11 |