FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10885862284532 · Model: 01-019-01-1017 · Exactech, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10885862284532
Version / Model
01-019-01-1017
Catalog Number
01-019-01-1017
Company Name
Exactech, Inc.
Labeler DUNS
157565946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-25
Public Version
1
Public Version Date
2022-09-02
Public Version Status
New
Public Device Record Key
5eeb7363-256e-4e62-817f-259ccb9c4f24

Device Description

17mm REVISION STEM REAMER

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
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
45115 Medullary canal orthopaedic reamer, rigid

Identifiers

Type ID
Primary 10885862284532

Premarket Submissions

Submission Number Supplement Number
K150066 000
K181532 000

Device Sizes

Type Value Unit Text
Outer Diameter 17 Millimeter