FDA UDI Not in Commercial Distribution 🇺🇸 United States

trUpoint ARCH Replacement Kit

DI: 00841439111819 · Model: MTHF225 · MEDTEC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
trUpoint ARCH Replacement Kit
Primary DI
00841439111819
Version / Model
MTHF225
Catalog Number
MTHF225
Company Name
MEDTEC, INC.
Labeler DUNS
103977526
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-08
Public Version
4
Public Version Date
2022-08-11
Public Version Status
Update
Public Device Record Key
3840093d-9593-48c5-9f05-20d6fb2b4961
Distribution End Date
2019-05-20

Device Description

Disposable non-sterile putty (6) for use with trUpoint ARCH

Device Characteristics

Single Use
Yes
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
No
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
61128 Stereotactic radiosurgical/radiotherapy arch head frame

Identifiers

Type ID
Primary 00841439111819

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K132908 000

Device Sizes

Type Value Unit Text
Width 3.75 Inch
Length 4.875 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Storage Environment Temperature
Temperature Range
High: 73 Degrees Fahrenheit