FDA UDI In Commercial Distribution 🇺🇸 United States

Splash®

DI: D813SPD19070 · Model: SPD1907 · DEN-MAT HOLDINGS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Splash®
Primary DI
D813SPD19070
Version / Model
SPD1907
Catalog Number
SPD1907
Company Name
DEN-MAT HOLDINGS, LLC
Labeler DUNS
809857704
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-13
Public Version
2
Public Version Date
2022-10-31
Public Version Status
Update
Public Device Record Key
10c9cc16-dd20-4a40-94c0-3ec4d6f2a90a

Device Description

SPLASH LITE REG CART 5pc

Device Characteristics

Single Use
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ELW Material, Impression

GMDN Terms

Code Name
35866 Silicone dental impression material

Identifiers

Type ID
Primary D813SPD19070

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not expose to direct sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit