← Back to catalogue

MobiliT Cup

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name
MobiliT Cup FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
ECiMa™ insert for 28 mm head - Diam. 64 FDA UDI
Model / Reference
HDM2864 FDA UDI
Description
ECiMa™ insert for 28 mm head - Diam. 64 FDA UDI

Identifiers

Catalog Number
HDM2864 FDA UDI
Primary DI / UDI-DI
05056139239250 FDA UDI
510(k) Number
K191831 FDA UDI
FDA Product Code
LZO FDA UDI
MEH FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Non-constrained polyethylene acetabular liner

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

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Corin Ltd

Sources (1)

  • FDA UDI 64f8a4dc-d547-41f5-a294-1fecda35196a 36 fields · synced May 30, 2026