FDA UDI In Commercial Distribution 🇺🇸 United States

MRH

DI: 07613327045321 · Model: 6481-3-112 · Howmedica Osteonics Corp.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MRH
Primary DI
07613327045321
Version / Model
6481-3-112
Catalog Number
6481-3-112
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2023-12-08
Public Version Status
Update
Public Device Record Key
38b6a4dc-f4ea-416c-9707-aa2e825b001b

Device Description

MRH Knee Tibial Baseplate

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KRO PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

GMDN Terms

Code Name
33692 Rotating hinged total knee prosthesis

Identifiers

Type ID
Primary 07613327045321

Premarket Submissions

Submission Number Supplement Number
K002552 000
K223069 000
K994207 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: MED-2