FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982031365 · Model: 02.111.210 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982031365
Version / Model
02.111.210
Catalog Number
02111210
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2022-04-28
Public Version Status
Update
Public Device Record Key
dde4ca2d-e4f2-4017-a796-6f9a2d06e1f9

Device Description

6.5MM MIDFOOT FUSION BOLT 110MM

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
HWC Screw, fixation, bone

GMDN Terms

Code Name
16077 Orthopaedic bone bolt

Identifiers

Type ID
Secondary H679021112100
Primary 10886982031365

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K081071 000