← Back to catalogue

ZEISS Axio Lab

FDA UDI

Class I (US FDA UDI)

by Carl Zeiss Suzhou Co., Ltd.

Identity

Trade Name
ZEISS Axio Lab FDA UDI
Generic Name
Basic light microscope FDA UDI
Model / Reference
Axio Lab.A1 FDA UDI

Identifiers

Catalog Number
430037-9020-000 FDA UDI
Primary DI / UDI-DI
06909262200125 FDA UDI
FDA Product Code
MTX FDA UDI
GMDN Term
Basic light microscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.6190 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: Basic light microscope

ZEISS Axio Lab by Carl Zeiss Suzhou Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic light microscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 5ce33735-90c7-496c-9e76-4a573f8227ef 35 fields · synced May 30, 2026