FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886705023202 · Model: 260003 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886705023202
Version / Model
260003
Catalog Number
260003
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
db340f85-44db-4aca-8b2b-386a265981a8

Device Description

Hip Blade Curved

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44052 Orthopaedic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 10886705023202

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
High: 80 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
High: 26 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
High: 26 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
High: 80 Degrees Fahrenheit