FDA UDI In Commercial Distribution 🇺🇸 United States

AcuMatch

DI: 10885862018137 · Model: 115-03-45 · Exactech, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AcuMatch
Primary DI
10885862018137
Version / Model
115-03-45
Catalog Number
115-03-45
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
fd1d5d37-cc01-4b6d-a3e2-c1acd27b92a6

Device Description

ACUMATCH COLLARED 12/14 LARGE NECK TRIAL

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 10885862018137

Device Sizes

Type Value Unit Text
Device Size Text, specify LARGE
Device Size Text, specify 12/14