FDA UDI In Commercial Distribution 🇺🇸 United States

RELIEVA SPINPLUS NAV

DI: 10705031241008 · Model: RSP0516MFSN · ACCLARENT, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RELIEVA SPINPLUS NAV
Primary DI
10705031241008
Version / Model
RSP0516MFSN
Catalog Number
RSP0516MFSN
Company Name
ACCLARENT, INC.
Labeler DUNS
361092450
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-09
Public Version
6
Public Version Date
2020-01-22
Public Version Status
Update
Public Device Record Key
272c61ba-2c75-41d7-be90-3a3c2ae879ac

Device Description

RELIEVA SPINPLUS NAV BALLOON SINUPLASTY SYSTEM, 5X16MM, 3 GUIDE KIT

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
LRC INSTRUMENT, ENT MANUAL SURGICAL
PGW Ear, Nose, and Throat Stereotaxic Instrument

GMDN Terms

Code Name
48140 Nasal/paranasal balloon catheter

Identifiers

Type ID
Package 20705031241005
Primary 10705031241008

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171687 000

Storage Conditions

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