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Lip Retractor

FDA UDI

Class I (US FDA UDI)

by Gestenco International AB

Identity

Trade Name
Lip Retractor FDA UDI
Generic Name
Hand-held dental retractor FDA UDI
Model / Reference
LR-00-02 FDA UDI

Identifiers

Catalog Number
LR-00-02 FDA UDI
Primary DI / UDI-DI
07333117000179 FDA UDI
FDA Product Code
EIF FDA UDI
GMDN Term
Hand-held dental retractor 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

Yes

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

Category: Hand-held dental retractor

Lip Retractor by Gestenco International AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held dental retractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de55eb2d-c8b8-44b7-b03b-079c413670c6 33 fields · synced May 30, 2026