FDA UDI In Commercial Distribution 🇺🇸 United States

COE®

DI: 10386040000734 · Model: 260211 · Gc America Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
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
COE®
Primary DI
10386040000734
Version / Model
260211
Catalog Number
260211
Company Name
Gc America Inc.
Labeler DUNS
005473608
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-07
Public Version
1
Public Version Date
2022-07-15
Public Version Status
New
Public Device Record Key
bd5eda12-c605-4441-836f-e848dcf47cc1

Device Description

COE® Regular-Perforated, Individual Tray, #21 Lower

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EBH MATERIAL, IMPRESSION TRAY, RESIN

GMDN Terms

Code Name
35850 Dental impression tray, reusable

Identifiers

Type ID
Package 40386040000735
Package 20386040000731
Primary 10386040000734

Customer Contacts