FDA UDI In Commercial Distribution 🇺🇸 United States

Synex

DI: 10705034753102 · Model: 04.807.245 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Synex
Primary DI
10705034753102
Version / Model
04.807.245
Catalog Number
04807245
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
5
Public Version Date
2022-05-27
Public Version Status
Update
Public Device Record Key
8bd7d5b8-9009-4d4a-94a2-7560863f9a6d

Device Description

SYNEX(TM) W/LRG ENDPLATE/OPEN -6 DEG/45MM-73MM HEIGHT (TI)

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Secondary H981048072450
Primary 10705034753102

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K003836 000