FDA UDI In Commercial Distribution 🇺🇸 United States

LCP

DI: 10886982222992 · Model: 442.507 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LCP
Primary DI
10886982222992
Version / Model
442.507
Catalog Number
442507
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
8
Public Version Date
2024-02-27
Public Version Status
Update
Public Device Record Key
2f2ac00b-4583-4d6a-9c4a-0744859aa9d5

Device Description

2.4MM TI LCP(TM) DISTAL RADIUS L-PLATE/-90DEG 3H HD/4H SHAFT

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

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Secondary H6794425070
Primary 10886982222992

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K012114 000
K091644 000