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Flow Dental

FDA UDI

Class I (US FDA UDI)

by DuPhaMed B.V.

Identity

Trade Name
Flow Dental FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Confee Ears Disposable ear sleeves for CBCT exams FDA UDI
Model / Reference
Earflow34 FDA UDI
Description
Confee Ears Disposable ear sleeves for CBCT exams FDA UDI

Identifiers

Catalog Number
81500 FDA UDI
Primary DI / UDI-DI
08717228442537 FDA UDI
FDA Product Code
EGZ FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.1905 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Category: Medical equipment/instrument drape, single-use

Flow Dental by DuPhaMed B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DuPhaMed B.V.

Sources (1)

  • FDA UDI 6ca0df73-bdc8-4017-8a5b-2b0c0d656cd9 34 fields · synced Jun 6, 2026