FDA UDI In Commercial Distribution 🇺🇸 United States

RESTORE

DI: 10886705005574 · Model: 219302 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RESTORE
Primary DI
10886705005574
Version / Model
219302
Catalog Number
219302
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
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
8d3c06ac-0e16-46cf-99f7-a7f69fdf46bd

Device Description

RESTORE FLAT RASP

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
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 10886705005574

Customer Contacts