FDA UDI
In Commercial Distribution
🇺🇸 United States
ACCLARENT PIVOT
DI: 10705031465572
·
Model: PVT0616L
·
ACCLARENT, INC.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- ACCLARENT PIVOT
- Primary DI
- 10705031465572
- Version / Model
- PVT0616L
- Catalog Number
- PVT0616L
- Company Name
- ACCLARENT, INC.
- Labeler DUNS
- 361092450
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2020-10-01
- Public Version
- 1
- Public Version Date
- 2020-10-09
- Public Version Status
- New
- Public Device Record Key
- ab564df3-9536-449b-9d39-7ed44ce78b51
Device Description
ACCLARENT PIVOT Illumination Balloon Dilation System
Device Characteristics
- Single Use
- Yes
- 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
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| PNZ | Eustachian tube balloon dilation device | Ear, Nose, Throat | 874.4180 | 2 |
| PGW | Ear, Nose, and Throat Stereotaxic Instrument | Neurology | 882.4560 | 2 |
| LRC | INSTRUMENT, ENT MANUAL SURGICAL | Ear, Nose, Throat | 874.4420 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 10718 | Eustachian catheter, single-use | A long, flexible tube used for middle ear drainage and/or temporary equalization of the pressure on both sides of the eardrum via insufflation. The distal tip is passed along the floor of the nose and guided into the Eustachian tube; air may be blown through the device and into the middle ear. It is typically made of plastic. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 20705031465579 | GS1 | BOX | 5 | In Commercial Distribution | |
| Primary | 10705031465572 | GS1 |
Customer Contacts
- Phone
- +1(650)687-5888
- [email protected]
- Phone
- +1(877)775-2789
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K201115 | 000 |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- Store in a cool, dry place.