FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982276704 · Model: 03.133.399 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982276704
Version / Model
03.133.399
Catalog Number
03133399
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-15
Public Version
2
Public Version Date
2022-05-02
Public Version Status
Update
Public Device Record Key
e36e96d7-e882-4a4f-8715-86ce5845b020

Device Description

LCP® PROX TIB LW BND TEM 6H /L ANATOMIC TEMPLATE

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
Yes
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
HWT TEMPLATE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Direct Marking 07612334149466
Primary 10886982276704

Customer Contacts