FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982072344 · Model: 03.111.036 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982072344
Version / Model
03.111.036
Catalog Number
03111036
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
7
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
60524a88-3cda-438e-8fa8-a3998cc7d330

Device Description

15MM REAMING GUIDE F/2.4MM VAL INTERCARPAL FUSION PLATE

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
HWC Screw, fixation, bone
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Secondary H679031110360
Primary 10886982072344
Direct Marking 07611819415096

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K103243 000