FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00888233025201 · Model: 7014-3266 · BIOMET MICROFIXATION, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00888233025201
Version / Model
7014-3266
Catalog Number
7014-3266
Company Name
BIOMET MICROFIXATION, INC
Labeler DUNS
046189866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-26
Public Version
1
Public Version Date
2020-07-06
Public Version Status
New
Public Device Record Key
8da04ee4-8959-4d91-9a61-85c09d25a751

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NEA CEMENT, EAR, NOSE AND THROAT

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 00888233025201

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K042516 000