FDA UDI In Commercial Distribution 🇺🇸 United States

Patient Vest Kit

DI: 20613031829201 · Model: 920 · Gentherm Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Patient Vest Kit
Primary DI
20613031829201
Version / Model
920
Catalog Number
82920
Company Name
Gentherm Medical, LLC
Labeler DUNS
004249462
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2017-08-30
Public Version
4
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
707d3dee-b22f-4802-8247-7081b4f628d4

Device Description

Thermal Regulating System

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
DWJ System, Thermal Regulating

GMDN Terms

Code Name
61251 External circulating-fluid core temperature regulation system pad, single-use

Identifiers

Type ID
Primary 20613031829201
Unit of Use 10613031829204

Customer Contacts

Device Sizes

Type Value Unit Text
Depth 3.0 Inch
Width 11.0 Inch
Length 14.25 Inch
Weight 0.62 Pound

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-40 – 150 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
-40 – 65.6 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
59 – 86 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
15 – 30 Degrees Celsius