FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20886982198676 · Model: 392.18 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
20886982198676
Version / Model
392.18
Catalog Number
39218
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2022-05-02
Public Version Status
Update
Public Device Record Key
57d415f6-7b9f-4d35-9ed7-df6b7bdee9fd

Device Description

PROTECTIVE CAPS FOR KIRSCHNER WIRES

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
LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE

GMDN Terms

Code Name
35647 External orthopaedic fixation system, reusable

Identifiers

Type ID
Secondary H679392180
Primary 20886982198676
Unit of Use 80886982198678

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K950384 000