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Rss-Sea

FDA UDI

Class I (US FDA UDI)

by Quality Aspirators, Inc.

Identity

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

Identifiers

Catalog Number
300-10152 FDA UDI
Primary DI / UDI-DI
00814005023625 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

Rss-Sea 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 a0f3ca9e-f2e5-44cf-94e2-1b89d958cf65 34 fields · synced May 30, 2026