FDA UDI In Commercial Distribution 🇺🇸 United States

Exergen DermaTemp

DI: 10834098000355 · Model: Dermatemp 1001 · EXERGEN CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Exergen DermaTemp
Primary DI
10834098000355
Version / Model
Dermatemp 1001
Catalog Number
104910
Company Name
EXERGEN CORPORATION
Labeler DUNS
061266060
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
65a38472-5f4b-491d-a373-8d7832ce9e92

Device Description

Dermatemp 1001 LN

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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
17888 Infrared patient thermometer, skin

Identifiers

Type ID
Primary 10834098000355

Customer Contacts

Phone
617-923-9900

Premarket Submissions

Submission Number Supplement Number
K873010 000