FDA UDI Not in Commercial Distribution 🇺🇸 United States

EZSTART

DI: 20845854001056 · Model: EZ0730T · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
EZSTART
Primary DI
20845854001056
Version / Model
EZ0730T
Catalog Number
EZ0730T
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-16
Public Version
9
Public Version Date
2026-04-01
Public Version Status
Update
Public Device Record Key
c41e22d6-974f-488c-a5fd-4bceb2818c0c
Distribution End Date
2026-04-01

Device Description

EZSTART INTERFERENCE SCREW, 7 MM X 30 MM

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, fixation, bone

GMDN Terms

Code Name
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Primary 20845854001056
Package 30845854001053

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 7mm x 30mm