FDA UDI In Commercial Distribution 🇺🇸 United States

Full XPE Cup

DI: 04719886894332 · Model: 9206-5032-TB · UNITED ORTHOPEDIC CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Full XPE Cup
Primary DI
04719886894332
Version / Model
9206-5032-TB
Catalog Number
9206-5032-TB
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-08
Public Version
1
Public Version Date
2023-06-16
Public Version Status
New
Public Device Record Key
950df462-43db-40d6-92bb-2962cd212cf7

Device Description

Cup pusher head, 32mm

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
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 04719886894332

Customer Contacts