FDA UDI In Commercial Distribution 🇺🇸 United States

C-Warmer

DI: 08800017901930 · Model: Dual · DXM CO., LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
C-Warmer
Primary DI
08800017901930
Version / Model
Dual
Company Name
DXM CO., LTD
Labeler DUNS
688797315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-15
Public Version
1
Public Version Date
2024-07-23
Public Version Status
New
Public Device Record Key
5818fa63-0a24-4626-83fc-4d49c096ac31

Device Description

C-Warmer is designed to enhance both the doctor' and the patiends'. A themostatically-controlled cartridge/composite warmer significantly reduces curing time with more flowability of composites and conveniently warms anesthetics and composites in one locations.

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EFC Warmer, Anesthetic Tube

GMDN Terms

Code Name
31810 Anaesthesia warmer

Identifiers

Type ID
Primary 08800017901930