FDA UDI In Commercial Distribution 🇺🇸 United States

RediFoam™

DI: 00841439110904 · Model: MTFA41B · MEDTEC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RediFoam™
Primary DI
00841439110904
Version / Model
MTFA41B
Catalog Number
MTFA41B
Company Name
MEDTEC, INC.
Labeler DUNS
103977526
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-02
Public Version
7
Public Version Date
2023-07-26
Public Version Status
Update
Public Device Record Key
692025a0-cc3c-4e9f-88ec-750cc618e4f0

Device Description

Two-part Foaming Agent Part A (21.8oz) and Foaming Agent Part B (24.6oz)

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYE Accelerator, linear, medical

GMDN Terms

Code Name
40894 Patient positioning foam mould kit

Identifiers

Type ID
Primary 00841439110904

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K951808 000

Device Sizes

Type Value Unit Text
Width 4.1 Centimeter
Length 19.4 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Fragile. Flammable, keep away from fire or flame. Keep away from sunlight.
Type
Storage Environment Temperature
Temperature Range
52 – 85 Degrees Fahrenheit