FDA UDI In Commercial Distribution 🇺🇸 United States

AcuMatch

DI: 10885862012760 · Model: 103-44-01 · Exactech, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AcuMatch
Primary DI
10885862012760
Version / Model
103-44-01
Catalog Number
103-44-01
Company Name
Exactech, Inc.
Labeler DUNS
157565946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-28
Public Version
1
Public Version Date
2022-08-05
Public Version Status
New
Public Device Record Key
db3afe4d-d741-4d28-85dd-4371b38df496

Device Description

DISASSEMBLY TOOL, BIPOLAR

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
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

GMDN Terms

Code Name
47866 Orthopaedic implant/instrument dismantling device

Identifiers

Type ID
Primary 10885862012760

Premarket Submissions

Submission Number Supplement Number
K905370 000