FDA UDI In Commercial Distribution 🇺🇸 United States

WAVE

DI: 09336472013547 · Model: 7520003 · SDI LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WAVE
Primary DI
09336472013547
Version / Model
7520003
Catalog Number
7520003
Company Name
SDI LIMITED
Labeler DUNS
753221852
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-09
Public Version
1
Public Version Date
2025-01-17
Public Version Status
New
Public Device Record Key
926944e9-89fb-47ea-88f0-5e46c53881d0

Device Description

WAVE MV 20 COMP A3

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
No
Sterilization Prior Use
No

Product Codes

Code Name
EBF Material, Tooth Shade, Resin

GMDN Terms

Code Name
35870 Dental composite resin

Identifiers

Type ID
Primary 09336472013547

Premarket Submissions

Submission Number Supplement Number
K973091 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Storage conditions 10°C - 25°C (50 - 77°F) Recommended Cool Room Storage Do not refrigerate SDI composite products.