← Back to catalogue

Defend

FDA UDI

Class II (US FDA UDI)

by Young Mydent, Llc

Identity

Trade Name
Defend FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Model / Reference
BR-9002 FDA UDI

Identifiers

Primary DI / UDI-DI
00816577020149 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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

No

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: Silicone dental impression material

Defend by Young Mydent, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Young Mydent, Llc

Sources (1)

  • FDA UDI 9f19bb8e-ae5e-4ede-bebf-15b9d7d8cb37 32 fields · synced May 30, 2026