FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10885862282989 · Model: 01-011-30-2245 · Exactech, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10885862282989
Version / Model
01-011-30-2245
Catalog Number
01-011-30-2245
Company Name
Exactech, Inc.
Labeler DUNS
157565946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-19
Public Version
1
Public Version Date
2022-09-27
Public Version Status
New
Public Device Record Key
5ea67113-589b-45a2-90fc-109c6866263d

Device Description

MONOBLOCK REVISION STEM TRIAL, 30x245

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
HWT TEMPLATE

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Primary 10885862282989

Device Sizes

Type Value Unit Text
Length 245 Millimeter
Outer Diameter 30 Millimeter