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Bite Block

FDA UDI

Class I (US FDA UDI)

by Hager Worldwide, Inc.

Identity

Trade Name
Bite Block FDA UDI
Generic Name
Dental cheek retractor, professional, reusable FDA UDI
Device Name
Bite-Block Green (BX/4) 2/Large , 2/Small FDA UDI
Model / Reference
605211 FDA UDI
Description
Bite-Block Green (BX/4) 2/Large , 2/Small FDA UDI

Identifiers

Primary DI / UDI-DI
D2486052111 FDA UDI
FDA Product Code
EIF FDA UDI
GMDN Term
Dental cheek retractor, professional, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental cheek retractor, professional, reusable

Bite Block by Hager Worldwide, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental cheek retractor, professional, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a7c4bdd1-a938-4a78-ade1-31f0ee246bc6 34 fields · synced Jun 9, 2026