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Bebeonkers I

FDA UDI

Class II (US FDA UDI)

by Small Beginnings, Inc.

Identity

Trade Name
Bebeonkers I FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
Device Name
The Bebeonkers I Oral/Nasal Suction Device is intended to be attached to wall suction and used as an oral or nasal cavity evacuator to remove secretions and maintain a clear airway. FDA UDI
Model / Reference
16-1 FDA UDI
Description
The Bebeonkers I Oral/Nasal Suction Device is intended to be attached to wall suction and used as an oral or nasal cavity evacuator to remove secretions and maintain a clear airway. FDA UDI

Identifiers

Catalog Number
16-1 FDA UDI
Primary DI / UDI-DI
00815090010057 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

Category: Surgical/emergency suction cannula, non-illuminating, reusable

Bebeonkers I by Small Beginnings, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b2fea0e8-81f4-4f57-a648-822eb80e1d11 36 fields · synced May 30, 2026