FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982001382 · Model: E5213-50 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982001382
Version / Model
E5213-50
Catalog Number
E521350
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-20
Public Version
3
Public Version Date
2018-06-26
Public Version Status
Update
Public Device Record Key
9e1e650d-467f-4f61-8d11-256bf3170e2b

Device Description

TRIAL GLENOID SIZE 50

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 07611819943728
Secondary H679E5213500O
Primary 10886982001382

Customer Contacts