FDA UDI In Commercial Distribution 🇺🇸 United States

LCP

DI: 10886982072610 · Model: 03.111.903 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
LCP
Primary DI
10886982072610
Version / Model
03.111.903
Catalog Number
03111903
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
2022-04-28
Public Version Status
Update
Public Device Record Key
76d9bc99-0169-41cb-a6f9-e9139be98d0e

Device Description

DRILL TEMPLATE F/2.7MM LCP ULNA OSTEOTOMY PL F/4.0MM

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 H679031119030
Primary 10886982072610
Direct Marking 07611819414488

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113364 000