FDA UDI In Commercial Distribution 🇺🇸 United States

AIRvance™

DI: 00643169107779 · Model: 76310200M · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AIRvance™
Primary DI
00643169107779
Version / Model
76310200M
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-22
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
c9b0ce25-f9fa-44c9-b904-cb576cc35f38

Device Description

BONE SCREW 76310200M AIRVANCE

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LRK Device, anti-snoring

GMDN Terms

Code Name
61483 Sleep apnoea tongue implant, non-bioabsorbable

Identifiers

Type ID
Primary 00643169107779

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K981677 000