FDA UDI In Commercial Distribution 🇺🇸 United States

XRL

DI: 10705034755243 · Model: 08.807.205S · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
XRL
Primary DI
10705034755243
Version / Model
08.807.205S
Catalog Number
08807205S
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
2022-04-26
Public Version Status
Update
Public Device Record Key
a78219ab-d4f1-43e2-bb4f-8dea37ebcf29

Device Description

XRL MEDIUM CENTRAL BODY 25MM-33MM HEIGHT-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
No

Product Codes

Code Name
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Secondary H98108807205S0
Primary 10705034755243

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K103320 000