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Apoteca

FDA UDI

Class II (US FDA UDI)

by Aea Srl

Identity

Trade Name
APOTECA FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
I.V. Transfer Set FDA UDI
Model / Reference
ADY1100CF FDA UDI
Description
I.V. Transfer Set FDA UDI

Identifiers

Primary DI / UDI-DI
05060304050120 FDA UDI
510(k) Number
K132011 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Fluid transfer set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Fluid transfer set, general-purpose

Apoteca by Aea Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluid transfer set, general-purpose.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aea Srl

Sources (1)

  • FDA UDI 8262a2a0-cae3-4f17-8fae-46e1dbe3bbd0 34 fields · synced May 30, 2026