FDA UDI
In Commercial Distribution
🇺🇸 United States
Axonics
DI: 10810005340103
·
Model: 2301
·
AXONICS MODULATION TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Axonics
- Primary DI
- 10810005340103
- Version / Model
- 2301
- Catalog Number
- 2301
- Company Name
- AXONICS MODULATION TECHNOLOGIES, INC.
- Labeler DUNS
- 079562449
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2019-09-23
- Public Version
- 1
- Public Version Date
- 2019-10-01
- Public Version Status
- New
- Public Device Record Key
- 602f08a3-8e4f-4460-b769-26623bb0d121
Device Description
Remote Control
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- Yes
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| EZW | Stimulator, Electrical, Implantable, For Incontinence | Gastroenterology, Urology | 876.5270 | 3 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 61396 | Implantable incontinence-control electrical stimulation system programmer, battery-powered | A portable, battery-powered external device intended to change, noninvasively, one or more of the operating parameters (the programs) of an implanted incontinence-control electrical stimulation system pulse generator. It includes controls (e.g., graphical user interface), integrated software, and a wireless communication transmitter and receiver. It will typically also provides historic and/or current information regarding the performance of the implant. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 10810005340103 | GS1 |
Customer Contacts
- Phone
- +1 (877) 929-6642
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| P190006 | 000 |