Pomee

FDA UDI

Class I (US FDA UDI)

by Pomee Corporation

Identity

Trade Name: Pomee FDA UDI
Generic Name: Dental surgical probe, reusable FDA UDI
Device Name: Explorer D.E #6 FDA UDI
Model / Reference: 704-860 FDA UDI
Description: Explorer D.E #6 FDA UDI

Identifiers

Catalog Number: 704-860 FDA UDI
Primary DI / UDI-DI: G1577048600 FDA UDI
FDA Product Code: EIX FDA UDI
GMDN Term: Dental surgical probe, 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

Yes

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental surgical probe, reusable

Pomee by Pomee Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Pomee Corporation

Sources (1)

FDA UDI 04779386-c118-4def-bb29-dacbf5e25c27 34 fields · synced Jun 1, 2026