FDA UDI In Commercial Distribution 🇺🇸 United States

LCP

DI: 10886982033604 · Model: 02.112.119S · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LCP
Primary DI
10886982033604
Version / Model
02.112.119S
Catalog Number
02112119S
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
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
17a1bc91-ab37-4c46-b585-4ff4b068d805

Device Description

2.7MM/3.5MM LCP POSTLAT DSTL FIBULA PL 9H/LEFT/155MM-STER

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
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
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Secondary H67902112119S0
Primary 10886982033604

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K073460 000
K083213 000