FDA UDI Not in Commercial Distribution 🇺🇸 United States

MOSS

DI: 10705034299723 · Model: 275040800 · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MOSS
Primary DI
10705034299723
Version / Model
275040800
Catalog Number
275040800
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
7
Public Version Date
2019-05-31
Public Version Status
Update
Public Device Record Key
be8fa2c9-2a6f-4a2a-9ed0-9b20a41d9897
Distribution End Date
2019-05-31

Device Description

MOSS MIAMI MAGNUM SPINE SYSTEM ANTI-CROSS THREAD OUTER 6.35

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 10705034299723

Customer Contacts