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Af1000a-Si

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
AF1000A-SI FDA UDI
Generic Name
Laboratory liquid dispenser, electronic FDA UDI
Device Name
Microplate Dispenser FDA UDI
Model / Reference
AF1000A-SI FDA UDI
Description
Microplate Dispenser FDA UDI

Identifiers

Primary DI / UDI-DI
05700574035167 FDA UDI
FDA Product Code
JQW FDA UDI
GMDN Term
Laboratory liquid dispenser, electronic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2750 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laboratory liquid dispenser, electronic

Af1000a-Si by Agilent Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory liquid dispenser, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa75d1ed-cacc-42e9-97f7-fa291971a3e5 35 fields · synced May 30, 2026