FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10885862026118 · Model: 141-01-22 · Exactech, Inc.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10885862026118
Version / Model
141-01-22
Catalog Number
141-01-22
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
2
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
55090dc2-d162-404c-b508-9f5952cf1a5b

Device Description

LINER DRIVER HEAD, 22mm

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
MEH Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
OQI Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 10885862026118

Premarket Submissions

Submission Number Supplement Number
K173583 000
K182502 000

Device Sizes

Type Value Unit Text
Outer Diameter 22 Millimeter
Device Size Text, specify Spherical Diameter