FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982341198 · Model: SD03.111.907 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982341198
Version / Model
SD03.111.907
Catalog Number
SD03111907
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-10
Public Version
1
Public Version Date
2022-08-18
Public Version Status
New
Public Device Record Key
41223f7b-de56-490d-9144-735e8d95f425

Device Description

2.7MM LCP OSTEOTOMY GUIDE 3.0MM OBLIQUE CUT

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
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
HRS Plate, fixation, bone
HWC Screw, fixation, bone

GMDN Terms

Code Name
45109 Orthopaedic reamer guide

Identifiers

Type ID
Primary 10886982341198

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113364 000