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MobiliT Cup

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name
MobiliT Cup FDA UDI
Generic Name
Orthopaedic implant/instrument assembling device FDA UDI
Device Name
Impaction liner pistol FDA UDI
Model / Reference
MDM014 FDA UDI
Description
Impaction liner pistol FDA UDI

Identifiers

Catalog Number
MDM014 FDA UDI
Primary DI / UDI-DI
05056139223198 FDA UDI
510(k) Number
K191831 FDA UDI
FDA Product Code
LZO FDA UDI
MEH FDA UDI
GMDN Term
Orthopaedic implant/instrument assembling device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant/instrument assembling device

MobiliT Cup by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant/instrument assembling device.

Cleared under the same submission

K191831 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corin Ltd

Sources (1)

  • FDA UDI 977f14ab-a3fd-420a-a08b-317b99464db3 36 fields · synced Jun 8, 2026