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Coe®

FDA UDI

Class I (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
COE® FDA UDI
Generic Name
Dental impression tray, reusable FDA UDI
Device Name
COE® Regular Trays-Solid Set of 8 Solid, #s 101, 104, 107, 109, 120, 121, 122, 124 FDA UDI
Model / Reference
261018 FDA UDI
Description
COE® Regular Trays-Solid Set of 8 Solid, #s 101, 104, 107, 109, 120, 121, 122, 124 FDA UDI

Identifiers

Catalog Number
261018 FDA UDI
Primary DI / UDI-DI
10386040002332 FDA UDI
FDA Product Code
EBH FDA UDI
GMDN Term
Dental impression tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3670 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental impression tray, reusable

Coe® by Gc America Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental impression tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gc America Inc.

Sources (1)

  • FDA UDI 7130ec49-24f0-4153-a8d6-696838530f41 35 fields · synced May 31, 2026