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Fisherbrand

FDA UDI

Class I (US FDA UDI)

by Fisher Scientific Company L.l.c.

Identity

Trade Name
Fisherbrand FDA UDI
Generic Name
Carbon dioxide laboratory incubator FDA UDI
Device Name
ISOTEMP DH CO2 IR 120V FDA UDI
Model / Reference
FB3533DH FDA UDI
Description
ISOTEMP DH CO2 IR 120V FDA UDI

Identifiers

Catalog Number
11676603 FDA UDI
Primary DI / UDI-DI
00613647024416 FDA UDI
FDA Product Code
JTQ FDA UDI
GMDN Term
Carbon dioxide laboratory incubator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2540 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: Carbon dioxide laboratory incubator

Fisherbrand by Fisher Scientific Company L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide laboratory incubator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76989ea0-24f6-42bf-a1b4-a6382160de1f 35 fields · synced Jun 1, 2026