FDA UDI In Commercial Distribution 🇺🇸 United States

ACCLARENT PIVOT

DI: 20705031465609 · Model: PVT0616NZ · ACCLARENT, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACCLARENT PIVOT
Primary DI
20705031465609
Version / Model
PVT0616NZ
Catalog Number
PVT0616NZ
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
eb04089f-83b1-4194-a46c-21692f4e5fb9

Device Description

ACCLARENT PIVOT Navigation Balloon Dilation System - 1PK

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
MR Unsafe
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
PGW Ear, Nose, and Throat Stereotaxic Instrument
LRC INSTRUMENT, ENT MANUAL SURGICAL
PNZ Eustachian tube balloon dilation device

GMDN Terms

Code Name
10718 Eustachian catheter, single-use

Identifiers

Type ID
Primary 20705031465609

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201115 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place.