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Block-4-Bite

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Block-4-Bite FDA UDI
Generic Name
Head/neck procedure positioner FDA UDI
Device Name
Disposable X-Ray Bite Blocks FDA UDI
Model / Reference
BB-070(7070) FDA UDI
Description
Disposable X-Ray Bite Blocks FDA UDI

Identifiers

Catalog Number
BB-070(7070) FDA UDI
Primary DI / UDI-DI
D832BB07070701 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Head/neck procedure positioner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Head/neck procedure positioner

Block-4-Bite by Plasdent Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Head/neck procedure positioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 2e450645-4c81-48f1-be07-0e31805876bf 34 fields · synced Jun 6, 2026