FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034204635 · Model: 282110016 · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034204635
Version / Model
282110016
Catalog Number
282110016
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
2021-04-21
Public Version Status
Update
Public Device Record Key
7eedb8be-f842-4a91-a9f1-b51d4a2682bf
Distribution End Date
2018-07-31

Device Description

SURGICAL TITANIUM MESH ENDCAP HOLDER RING 16mm

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
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 10705034204635

Customer Contacts