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Ap209-01

FDA UDI

Class II (US FDA UDI)

by Eitan Medical Ltd

Identity

Trade Name
AP209-01 FDA UDI
Generic Name
Electric infusion pump administration set, single-use FDA UDI
Device Name
Spiral set FDA UDI
Model / Reference
12003-000-1027 FDA UDI
Description
Spiral set FDA UDI

Identifiers

Primary DI / UDI-DI
17290109155217 FDA UDI
510(k) Number
K192860 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Electric infusion pump administration set, single-use 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electric infusion pump administration set, single-use

Ap209-01 by Eitan Medical Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric infusion pump administration set, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eitan Medical Ltd

Sources (1)

  • FDA UDI eb06bf3a-abf1-46c0-8788-d2c2f9cd528f 34 fields · synced May 30, 2026