FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982189035 · Model: 314.742 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982189035
Version / Model
314.742
Catalog Number
314742
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-30
Public Version
4
Public Version Date
2022-04-29
Public Version Status
Update
Public Device Record Key
2127d30c-d263-424a-959e-1109a4823065

Device Description

DRIVE SHAFT-MINIMUM 360MM LENGTH-FOR USE WITH RIA

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
HTO REAMER
HRX ARTHROSCOPE

GMDN Terms

Code Name
35297 Medullary canal orthopaedic reamer, flexible

Identifiers

Type ID
Direct Marking 07611819739192
Secondary H6793147420
Primary 10886982189035

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K013527 000
K042899 000