Monty 3D Curved L

FDA UDI

Class I (US FDA UDI)

by REHAdapt Engineering GmbH & Co. KG

Identity

Trade Name: Monty 3D Curved L FDA UDI
Generic Name: Portable active medical device mount FDA UDI
Device Name: M3D two-tube wheelchair mount with curved tube. RotLok base with swivel function and UDS-DC. Dimensions (height x offset x tube 2): 760 x 300 x 400 mm (30 x 12 x 16"). Max. load capacity: 3.0 kg (6.6 lbs). Frame clamp not included. FDA UDI
Model / Reference: 11.6312 FDA UDI
Description: M3D two-tube wheelchair mount with curved tube. RotLok base with swivel function and UDS-DC. Dimensions (height x offset x tube 2): 760 x 300 x 400 mm (30 x 12 x 16"). Max. load capacity: 3.0 kg (6.6 lbs). Frame clamp not included. FDA UDI

Identifiers

Primary DI / UDI-DI: B8961163120 FDA UDI
FDA Product Code: KNO FDA UDI
GMDN Term: Portable active medical device mount FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3910 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Portable active medical device mount

Monty 3D Curved L by REHAdapt Engineering GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: REHAdapt Engineering GmbH & Co. KG

Sources (1)

FDA UDI fac20550-cfbf-4973-90e8-63161b78c727 33 fields · synced May 30, 2026