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Retractor, All Types,

FDA UDI

Class I (US FDA UDI)

by Retract Eez, Inc.

Identity

Trade Name
Retractor, All Types, FDA UDI
Generic Name
Dental cheek retractor, professional, reusable FDA UDI
Model / Reference
MFR #14072 FDA UDI

Identifiers

Primary DI / UDI-DI
00860009140608 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Liquid Chemical FDA UDI

Category: Dental cheek retractor, professional, reusable

Retractor, All Types, by Retract Eez, 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

Manufacturer
Retract Eez, Inc.

Sources (1)

  • FDA UDI 1e5e3298-1b85-4f01-80e5-7af560916a9d 32 fields · synced Jun 1, 2026