FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10886982241337 · Model: 5413-20/5-15 · SYNTHES (U.S.A.) LP
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982241337
Version / Model
5413-20/5-15
Catalog Number
541320515
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
2015-09-14
Public Version
5
Public Version Date
2019-09-02
Public Version Status
Update
Public Device Record Key
c6faf3ad-4da1-48b5-af13-fd69780af019
Distribution End Date
2019-09-01

Device Description

TI ECCENTER REVISION +15-STERILE

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
HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED
KWT PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED
MBF PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED

GMDN Terms

Code Name
60512 Shoulder humeral body prosthesis

Identifiers

Type ID
Secondary H6795413205150
Primary 10886982241337

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K072578 000