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Aboel

FDA UDI

Class I (US FDA UDI)

by Aboel Electronic Technology (shenzhen) Co., Ltd

Identity

Trade Name
ABOEL FDA UDI
Generic Name
Oral lavage system FDA UDI
Model / Reference
ABB889 FDA UDI

Identifiers

Primary DI / UDI-DI
06975815308891 FDA UDI
FDA Product Code
EFS FDA UDI
GMDN Term
Oral lavage system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6510 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

No

FDA UDI

Category: Oral lavage system

Aboel by Aboel Electronic Technology (shenzhen) Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oral lavage system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b4791e55-933c-40be-bd67-ac47c50fe299 32 fields · synced Jun 1, 2026