FDA UDI In Commercial Distribution 🇺🇸 United States

EXPLOR

DI: 00880304648968 · Model: IFS-204022 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EXPLOR
Primary DI
00880304648968
Version / Model
IFS-204022
Catalog Number
IFS-204022
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
e9212aab-3312-40df-b305-e804406f741c

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
MR Conditional
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
HRS PLATE, FIXATION, BONE
HWC Screw, fixation, bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00880304648968

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110201 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 2MM Ø 22MM LENGTH