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ANA 70 Duett 200

FDA UDI

Class II (US FDA UDI)

by Wykle Research, Inc.

Identity

Trade Name
ANA 70 Duett 200 FDA UDI
Generic Name
Dental amalgam FDA UDI
Model / Reference
1116100 FDA UDI

Identifiers

Primary DI / UDI-DI
00853383006554 FDA UDI
510(k) Number
K002808 FDA UDI
FDA Product Code
EJJ FDA UDI
GMDN Term
Dental amalgam FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

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 amalgam

ANA 70 Duett 200 by Wykle Research, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental amalgam.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 906a29e1-d78d-4505-9d91-659657a9335d 34 fields · synced May 30, 2026