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Extnd

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
EXTND FDA UDI
Generic Name
Dental cheek retractor, professional, reusable FDA UDI
Device Name
Double Ended Cheek Retractors, Large Size FDA UDI
Model / Reference
EX-9004 FDA UDI
Description
Double Ended Cheek Retractors, Large Size FDA UDI

Identifiers

Catalog Number
EX-9004 FDA UDI
Primary DI / UDI-DI
D832EX90041 FDA UDI
FDA Product Code
EIG 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental cheek retractor, professional, reusable

Extnd by Plasdent Corp. — 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

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 50e3bf9f-9b3a-47cd-a0ee-b45d2b193392 34 fields · synced May 30, 2026