FDA UDI In Commercial Distribution 🇺🇸 United States

CANCELLO-PURE

DI: 00889797040532 · Model: 4666H101 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CANCELLO-PURE
Primary DI
00889797040532
Version / Model
4666H101
Catalog Number
4666H101
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-17
Public Version
3
Public Version Date
2022-08-11
Public Version Status
Update
Public Device Record Key
e78817a1-0c92-4d0a-b650-94bf976ef4ce

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
47866 Orthopaedic implant/instrument dismantling device

Identifiers

Type ID
Primary 00889797040532

Customer Contacts