FDA UDI In Commercial Distribution 🇺🇸 United States

SURFIX®

DI: 10381780051794 · Model: FPOFND · NEWDEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SURFIX®
Primary DI
10381780051794
Version / Model
FPOFND
Company Name
NEWDEAL
Labeler DUNS
536935331
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-26
Public Version
4
Public Version Date
2023-02-06
Public Version Status
Update
Public Device Record Key
f9b41146-c158-4cc7-905d-4f3812ff4a81
Distribution End Date
2027-12-31

Device Description

The trial plate is used to define the correct position of the final POF implant.

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWT TEMPLATE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Secondary M248FPOFND1
Primary 10381780051794

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 24.00mm width; 88mm length; 2mm thickness; 12° bending angle