FDA UDI In Commercial Distribution 🇺🇸 United States

Comprehensive Reverse

DI: 00880304848344 · Model: SSI003433 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Comprehensive Reverse
Primary DI
00880304848344
Version / Model
SSI003433
Catalog Number
SSI003433
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-12
Public Version
4
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
5e6f27b3-a04f-4c83-8f4d-b66d12f2f9f4

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
PAO Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, Cemented
KES Coverslips, Microscope Slide

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 00880304848344

Customer Contacts