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Dh-Bb

FDA UDI

Class I (US FDA UDI)

by Quality Aspirators, Inc.

Identity

Trade Name
DH-BB FDA UDI
Generic Name
Dental suction system cannula, reusable FDA UDI
Device Name
DH-BB FDA UDI
Model / Reference
DH-BB FDA UDI
Description
DH-BB FDA UDI

Identifiers

Catalog Number
309-10016 FDA UDI
Primary DI / UDI-DI
00814005025025 FDA UDI
FDA Product Code
EHZ FDA UDI
GMDN Term
Dental suction system cannula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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
MRI Safety
MR Unsafe FDA UDI

Category: Dental suction system cannula, reusable

Dh-Bb by Quality Aspirators, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f272366d-82a5-4401-9d04-3d9b97d66796 34 fields · synced May 30, 2026