FDA UDI In Commercial Distribution 🇺🇸 United States

Arctic Blast

DI: D872AB10121 · Model: Arctic Blast · MARIE REIKO INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arctic Blast
Primary DI
D872AB10121
Version / Model
Arctic Blast
Company Name
MARIE REIKO INC
Labeler DUNS
033706171
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-15
Public Version
1
Public Version Date
2018-06-15
Public Version Status
New
Public Device Record Key
aa962c4e-a385-41be-9b93-c34d1c43d9f1

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EAT Tester, Pulp

GMDN Terms

Code Name
38787 Cryogenic spray, dental

Identifiers

Type ID
Primary D872AB10121