FDA UDI In Commercial Distribution 🇺🇸 United States

ProForm™ Thermoplastic

DI: 00841439113677 · Model: PRO339IM1832N · MEDTEC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ProForm™ Thermoplastic
Primary DI
00841439113677
Version / Model
PRO339IM1832N
Catalog Number
PRO339IM1832N
Company Name
MEDTEC, INC.
Labeler DUNS
103977526
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-12
Public Version
1
Public Version Date
2024-02-20
Public Version Status
New
Public Device Record Key
21249708-ef28-44ef-9c59-fc6ba271394a

Device Description

IMRT style 18 thermoplastic (3.2mm)

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
MR Safe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
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
IYE Accelerator, linear, medical
LNH System, nuclear magnetic resonance imaging

GMDN Terms

Code Name
40896 Patient positioning thermoplastic mould material

Identifiers

Type ID
Package 10841439113674
Primary 00841439113677

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180021 000

Storage Conditions

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