← Back to catalogue

Defend

FDA UDI

Class I (US FDA UDI)

by Young Mydent, Llc

Identity

Trade Name
Defend FDA UDI
Generic Name
Digital imaging cassette/storage phosphor screen, dental FDA UDI
Model / Reference
BF-8700 FDA UDI

Identifiers

Primary DI / UDI-DI
00816577022075 FDA UDI
FDA Product Code
IXC FDA UDI
GMDN Term
Digital imaging cassette/storage phosphor screen, dental FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1890 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Digital imaging cassette/storage phosphor screen, dental

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

Similar devices

Also classified as Digital imaging cassette/storage phosphor screen, dental.

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 76efb23c-fa96-4bbf-b01f-4b1653dfa721 32 fields · synced Jun 8, 2026