FDA UDI In Commercial Distribution 🇺🇸 United States

XRL

DI: 10705034723754 · Model: 03.807.601 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
XRL
Primary DI
10705034723754
Version / Model
03.807.601
Catalog Number
03807601
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
2022-06-01
Public Version Status
Update
Public Device Record Key
cd157b93-30e1-4903-8d44-6ed73368d322

Device Description

XRL LARGE TRIAL-INTEGRATED 23MM-26MM HEIGHT/0 DEG

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
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
44788 Spinal implant trial

Identifiers

Type ID
Secondary H981038076010
Primary 10705034723754
Direct Marking 07611819407008

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K103320 000