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DELTA TT Pro

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
DELTA TT Pro FDA UDI
Generic Name
Metallic acetabulum prosthesis FDA UDI
Device Name
Acetabular Cup (Ti6Al4V) Dia. 50 mm, for Liners size MEDIUM + FDA UDI
Model / Reference
5553.14.503 FDA UDI
Description
Acetabular Cup (Ti6Al4V) Dia. 50 mm, for Liners size MEDIUM + FDA UDI

Identifiers

Catalog Number
5553.14.503 FDA UDI
Primary DI / UDI-DI
08033390146043 FDA UDI
FDA Product Code
LPH FDA UDI
MBL FDA UDI
GMDN Term
Metallic acetabulum prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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

Category: Metallic acetabulum prosthesis

DELTA TT Pro by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic acetabulum prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI b3493fc7-46ef-4928-b3cd-c9a2c46e4146 35 fields · synced May 30, 2026