Molift

26 catalogue numbers from Molift Mover 180 complete excl. sling ba, listed by Etac A/S, Denmark, under Lift, Patient, Non-Ac-Powered. 71 manufacturers in China are registered for this product code.

Registry build 21.09.26
71manufacturers in China registered for this device type
26catalogue numbers in this listing
9recalls on this code

Who Else Makes It

Concentrated in Guangdong (32), Jiangsu (15), Zhejiang (7). 26 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FSA
Manufacturer City Province Registered as Device types
Mobility Source Medical Technology Co., Ltd. Foshan Guangdong Contract manufacturer 26
Jiangyin Huashi Medical Equipment Co., Ltd. Jiangyin Jiangsu Contract manufacturer 21
Hebei Jiede Medical Equipment Co., Ltd. Hengshui Hebei Contract manufacturer 20
Tops Medical Articles Industries Nantong Inc Qidong Jiangsu Contract manufacturer 17
Raise Medical Industries, Inc. Foshan Guangdong Contract manufacturer 16
Foshan Dongfang Medical Equipment Manufactory(Ltd) Foshan Guangdong Contract manufacturer 14
Genteel Homecare Products Co., Ltd. Foshan Guangdong Contract manufacturer 12
Dongguan Vigor Textile Co., Ltd. Dongguan Guangdong Contract manufacturer 11
Ningbo Kangmailong Medical Apparatus Co., Ltd. Cixi City, Ningbo Zhejiang Contract manufacturer 10
Ehob (Shanghai) Medical Products Co., Ltd. Pudong Shanghai Contract manufacturer 8
Jiangmen Jia Mei Medical Products Co., Ltd. Heshan Guangdong Contract manufacturer 8
Shanghai Ehob Health Care Products Co., Ltd. Shanghai Shanghai Contract manufacturer 8

Showing 12 of 71. All 71 manufacturers in China registered for Lift, Patient, Non-Ac-Powered

Record

Regulatory record for Molift
Listed by Etac A/S, Denmark
FDA product code FSA
Device type Lift, Patient, Non-Ac-Powered
Device class Class 1
Regulation 21 CFR 880.5510
Establishment Manufacturer
Premarket notification Exempt
Record published 2022-12-10

Specifications

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

Catalogue Numbers

Catalogue numbers for Molift
Catalogue number Size Status
Molift Mover 180 complete excl. sling bar In distribution
Molift QuickRaiser 205 Active In distribution
Molift AIR 205 Propulsion In distribution
Molift Quick Raiser 1 complete with U-shape arm In distribution
Molift Nomad complete SWL 205 kg In distribution
Molift Mover 180 compl excl. sling bar with 100mm Wheel In distribution
Molift Quick Raiser 2 complete with U-shape arm In distribution
Molift Mover 205 Standard complete excl. sling bar In distribution
Molift AIR 205 In distribution
Molift AIR 200 In distribution
Molift AIR 205 IRC In distribution
Molift AIR 300 In distribution
Molift Mover 300 low base walking bar In distribution
Molift Partner 255 Standard complete excl. sling bar In distribution
Molift AIR 300 Propulsion In distribution
Molift Quick Raiser 205 Active FL (Ø50/75mm) In distribution
Molift Mover 205 Low base complete excl. sling bar In distribution
Molift AIR 350 Tilt In distribution
Molift Partner 255 Low base complete excl. sling bar In distribution
Molift Partner 255 Low base with scale excl. sling bar In distribution
Molift AIR 350 In distribution
Molift Smart 150 complete incl. sling bar In distribution
Molift Mover 300 Low Base complete excl. sling bar In distribution
Molift Quick Raiser 205 Active FL (Ø75/100mm) In distribution
Molift Nomad complete SWL 255 kg In distribution
Molift AIR 500 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
EZ Way EZ WAY, Inc. 371
Handi-Move Sling Handi-Move 239
Arjo Sling Arjohuntleigh AB 195
Handicare Handicare USA, Inc. 166
Slings Joerns Healthcare 155
M-Series Savaria Concord Lift 100
GoLift Amico Mobility Solutions 87
Medline Medline Industries, Inc. 81
M-Series Savaria Concord Lifts Inc. 64
Monarch Savaria Concord Lifts Inc. 62
Apex Lifts Joerns Healthcare 58
Drive Drive DeVilbiss Healthcare 57

Showing 12 of 311. All products under Lift, Patient, Non-Ac-Powered

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Molift
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Etac A/S UDI-DI 2025-11-17 Class II Component design/selection A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformatio 95 units

Recalls

8 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2025-11-17 Class II Component design/selection A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformatio 25 units
2025-11-17 Class II Component design/selection A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformatio 64 units
2025-11-17 Class II Component design/selection A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformatio 71
2019-02-04 Class II Use error The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall. 427 total
2019-02-04 Class II Use error The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall. 427 (total)
2016-06-24 Class II Device Design Potential for the bolt on the suspension coupling on the Molift Air to come loose from the housing. 516 units (374 US) 2017-06-23
2013-02-15 Class II Employee error The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user. 7,555 units subject to review; US: 1,280 units – Foreign: 6, 2014-07-11
2013-02-15 Class II Employee error The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user. Subject to recall 1,460 units; US: 175 units; Foreign: 1,285 2014-07-11

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer