FDA UDI In Commercial Distribution 🇺🇸 United States

RESTORE

DI: 10886705005932 · Model: 219351 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RESTORE
Primary DI
10886705005932
Version / Model
219351
Catalog Number
219351
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
3
Public Version Date
2018-04-20
Public Version Status
Update
Public Device Record Key
28642451-1977-4475-873a-a0a4a3a9710b

Device Description

RESTORE TUNNEL NOTCHER

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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
34827 Tendon/ligament tunneller

Identifiers

Type ID
Primary 10886705005932

Customer Contacts