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Manus Medical, LLC

FDA UDI

Class II (US FDA UDI)

by Manus Medical, LLC

Identity

Trade Name
Manus Medical, LLC FDA UDI
Generic Name
Aspiration tray, single-use FDA UDI
Device Name
Loop Insertion Tray FDA UDI
Model / Reference
M400-20648 FDA UDI
Description
Loop Insertion Tray FDA UDI

Identifiers

Primary DI / UDI-DI
00811870037696 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Aspiration tray, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Aspiration tray, single-use

Manus Medical, LLC by Manus Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aspiration tray, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Manus Medical, LLC

Sources (1)

  • FDA UDI b51a50d6-8441-48fc-8138-e01af7e8860d 33 fields · synced May 30, 2026