FDA UDI In Commercial Distribution 🇺🇸 United States

Procheck

DI: 00642632016662 · Model: MT1P21-PRO · MICROLIFE USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Procheck
Primary DI
00642632016662
Version / Model
MT1P21-PRO
Company Name
MICROLIFE USA, INC.
Labeler DUNS
176387785
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-06
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
0778fd06-d540-40c4-979a-8c591e695196

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
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
FLL Thermometer, Electronic, Clinical

GMDN Terms

Code Name
14035 Intermittent electronic patient thermometer

Identifiers

Type ID
Package 20642632016666
Package 10642632016669
Primary 00642632016662