FDA UDI In Commercial Distribution 🇺🇸 United States

SURFIX®

DI: 10381780043287 · Model: MA010ND · NEWDEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SURFIX®
Primary DI
10381780043287
Version / Model
MA010ND
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
81f7ec75-17b0-4388-9c3b-82c1784b1ba3
Distribution End Date
2027-12-31

Device Description

The SURFIX® cutting guide is used to define he angle of the bone cutting and to guide the resection of a bone wedge when a closing wedge osteotomy is implemented.

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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Secondary M248MA010ND1
Primary 10381780043287

Customer Contacts