FDA UDI In Commercial Distribution 🇺🇸 United States

Comprehensive® Instrumentation

DI: 00887868469855 · Model: 110025762 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Comprehensive® Instrumentation
Primary DI
00887868469855
Version / Model
110025762
Catalog Number
110025762
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-24
Public Version
1
Public Version Date
2021-04-01
Public Version Status
New
Public Device Record Key
d282922c-7b88-4db4-9518-a138eaf85dff

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
PHX shoulder prosthesis, reverse configuration
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

GMDN Terms

Code Name
32845 Surgical depth gauge, reusable

Identifiers

Type ID
Primary 00887868469855

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080642 000
K120121 000
K132239 000
K193373 000