FDA UDI Not in Commercial Distribution 🇺🇸 United States

Epoca

DI: 10886982000682 · Model: E5113-12L · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Epoca
Primary DI
10886982000682
Version / Model
E5113-12L
Catalog Number
E511312L
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
5
Public Version Date
2019-03-25
Public Version Status
Update
Public Device Record Key
dec4b5ca-3899-4a4c-9e6b-310de2ce4563
Distribution End Date
2019-03-23

Device Description

TRIAL STEM EPOCA SIZE 12/LONG

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 07611819956889
Secondary H679E511312L0
Primary 10886982000682

Customer Contacts