FDA UDI In Commercial Distribution 🇺🇸 United States

EXPert

DI: 10886982066923 · Model: 03.010.004 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
EXPert
Primary DI
10886982066923
Version / Model
03.010.004
Catalog Number
03010004
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
f2c8369c-f4a2-4947-b484-4e3159cf3b6c

Device Description

COMPRESSION DEVICE/ FOR TI CANNULATED TIBIA NAILS-EX

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
JDS NAIL, FIXATION, BONE

GMDN Terms

Code Name
47875 Bone-nailing compression screw

Identifiers

Type ID
Secondary H679030100040
Primary 10886982066923
Direct Marking 07611819160385

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040762 000