What is FDA product code PUB?

This product code is the class II exempt counterpart of MQG, and was exempted, subject to the limitations of exemption, under the procedures established by the 21st Century Cures Act. This device type does not require premarket notification (510(k)) to market if it does not exceed the general limitations of exemption found in 21 CFR 884.9 and the specific limitations of exemption as stated in the Physical State field of this product code description.

Obstetrics & Gynecology › MiscellaneousAccessory, Assisted Reproduction, Exempt

Multiroom IVF Incubator

Name: Multiroom IVF incubator
Brand: Multiroom IVF incubator

The Esco Medical MIRI® M multiroom IVF incubators are intended to be used by trained healthcare professionals in the in vitro fertilisation (IVF) / assisted reproduction technology (ART)…

Registry build 21.09.26

The Esco Medical MIRI® M multiroom IVF incubators are intended to be used by trained healthcare professionals in the in vitro fertilisation (IVF) / assisted reproduction technology (ART) facilities to maintain and provide a stable culture environment with controlled temperature and CO2/O2 gas concentration for fertilised oocytes to the blastocyst stage during IVF / ART treatments and optionally to capture time lapse images of these during incubation.

3manufacturers in China registered for this device type

6catalogue numbers in this listing

Who Else Makes It

Concentrated in Hubei (1), Guangdong (1), Sichuan (1).

Chinese manufacturers registered for FDA product code PUB
Manufacturer	City	Province	Registered as	Device types
Wuhan Huchuang Union Technology Co., Ltd.	Wuhan	Hubei	Manufacturer	8
HUA YUE Medical Technology Co., Ltd.	Guangzhou	Guangdong	Manufacturer	7
MVE Cryogenic Biological Equipment (Chengdu) Co., Ltd.	Pidu District Chengdu	Sichuan	Manufacturer	3

Record

Regulatory record for Multiroom IVF incubator
Listed by	Esco Medical Technologies, UAB, Lithuania
FDA product code	PUB
Device type	Accessory, Assisted Reproduction, Exempt
Device class	Class 2
Regulation	21 CFR 884.6120
Establishment	Manufacturer
Premarket notification	Exempt
Record published	2026-01-14

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Prescription	Prescription only
Label carries	manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Multiroom IVF incubator
Catalogue number	Size	Status
MIRI Humidity		In distribution
MIRI II-12		In distribution
Mini MIRI Humidity		In distribution
MIRI M Chamber		In distribution
Mini MIRI Dry		In distribution
MIRI M Docking Station		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
K-Systems	Coopersurgical, Inc.	66
Fortuna	Research Instruments Ltd	28
Mars	Research Instruments Ltd	19
Multi-zone ART Workstation	Esco Medical Technologies, UAB	13
CT37 Incubator	Planer Limited	9
Titan	Research Instruments Ltd	7
K-Systems	Research Instruments Ltd	6
Hariomed	HUA YUE Medical Technology Co., Ltd.	4
G185	Research Instruments Ltd	4
PHCbi	PHC Corporation	3
BT37	Planer Limited	2
Aire~Lifeline	Lifeaire Systems	2

Showing 12 of 27. All products under Accessory, Assisted Reproduction, Exempt

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.