FDA UDI In Commercial Distribution 🇺🇸 United States

Thermoplastic Frame

DI: 00841439102008 · Model: 20CFHNPSUB1P · MEDTEC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Thermoplastic Frame
Primary DI
00841439102008
Version / Model
20CFHNPSUB1P
Catalog Number
20CFHNPSUB1P
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
5
Public Version Date
2020-03-19
Public Version Status
Update
Public Device Record Key
298b47d3-b482-49f7-889a-412d66a1f6df

Device Description

Reloadable pediatric Type-S™ frame

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
IYE Accelerator, linear, medical

GMDN Terms

Code Name
40897 Indexed-immobilization patient positioning system

Identifiers

Type ID
Primary 00841439102008

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080072 000
K933227 000

Device Sizes

Type Value Unit Text
Width 45.2 Centimeter
Length 48.5 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight