FDA UDI In Commercial Distribution 🇺🇸 United States

ProForm™ Thermoplastic

DI: 00841439113172 · Model: PRO330IM1832 · MEDTEC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ProForm™ Thermoplastic
Primary DI
00841439113172
Version / Model
PRO330IM1832
Catalog Number
PRO330IM1832
Company Name
MEDTEC, INC.
Labeler DUNS
103977526
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-22
Public Version
3
Public Version Date
2022-08-11
Public Version Status
Update
Public Device Record Key
f2240129-2cef-4e20-8495-c6724957f934

Device Description

Head-only IMRT style 18 thermoplastic (3.2mm)

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
Direct Marking Exempt
Yes
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
LNH System, nuclear magnetic resonance imaging
IYE Accelerator, linear, medical

GMDN Terms

Code Name
40896 Patient positioning thermoplastic mould material

Identifiers

Type ID
Package 10841439113179
Primary 00841439113172

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180021 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 100 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight