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Aquaboss®

FDA UDI

Class II (US FDA UDI)

by B.Braun Avitum AG

Identity

Trade Name
Aquaboss® FDA UDI
Generic Name
Reverse-osmosis water purification system FDA UDI
Device Name
EcoRO Dia I 2800 HT NA FDA UDI
Model / Reference
LA1106282 FDA UDI
Description
EcoRO Dia I 2800 HT NA FDA UDI

Identifiers

Catalog Number
LA1106282 FDA UDI
Primary DI / UDI-DI
04046964859656 FDA UDI
FDA Product Code
FIP FDA UDI
GMDN Term
Reverse-osmosis water purification system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5665 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Reverse-osmosis water purification system

Aquaboss® by B.Braun Avitum AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse-osmosis water purification system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B.Braun Avitum AG

Sources (1)

  • FDA UDI 085d45e7-ddb1-4518-8e6a-77eb0017fb76 36 fields · synced Jun 8, 2026