FDA UDI In Commercial Distribution 🇺🇸 United States

2.7MM SYSTEM

DI: 00841036065638 · Model: 99-9956 · BIOMET MICROFIXATION, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
2.7MM SYSTEM
Primary DI
00841036065638
Version / Model
99-9956
Catalog Number
99-9956
Company Name
BIOMET MICROFIXATION, INC
Labeler DUNS
046189866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-17
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
c73cb781-37ca-4ae1-8826-9312398d933b

Device Description

CROSS-DRIVE EMERGENCY SCREW 3.2X16MM

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
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
JEY Plate, Bone

GMDN Terms

Code Name
46638 Craniofacial bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00841036065638

Customer Contacts

Phone
904-741-4400

Premarket Submissions

Submission Number Supplement Number
K854886 000