FDA UDI Not in Commercial Distribution 🇺🇸 United States

Posifix® Headrest

DI: 00841439101322 · Model: 305000 · MEDTEC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Posifix® Headrest
Primary DI
00841439101322
Version / Model
305000
Catalog Number
305000
Company Name
MEDTEC, INC.
Labeler DUNS
103977526
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-02
Public Version
6
Public Version Date
2019-08-30
Public Version Status
Update
Public Device Record Key
949491eb-de9e-4ea3-a178-50653726ecf8
Distribution End Date
2019-08-30

Device Description

Reusable non-sterile set of five supine headrests

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
LNH System, nuclear magnetic resonance imaging

GMDN Terms

Code Name
61132 Radiological headrest

Identifiers

Type ID
Primary 00841439101322

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K060737 000
K093738 000