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Implant Partners

FDA UDI

Class III (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Implant Partners FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
COCR SF FEM HEAD 36MM SLT TPR MED NK IMPLANT PARTNERS™ FDA UDI
Model / Reference
26000026WD FDA UDI
Description
COCR SF FEM HEAD 36MM SLT TPR MED NK IMPLANT PARTNERS™ FDA UDI

Identifiers

Catalog Number
26000026WD FDA UDI
Primary DI / UDI-DI
M68426000026WD1 FDA UDI
FDA Product Code
JDL FDA UDI
KWA FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
888.3320 FDA UDI
888.3330 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

Yes

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 36 Millimeter FDA UDI

Category: Metallic femoral head prosthesis

Implant Partners by MicroPort Orthopedics Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fe4176ab-96f6-4c3f-b4d2-2b22252d8941 36 fields · synced Jun 9, 2026