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Advantim

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Advantim FDA UDI
Generic Name
Knee femur stem prosthesis FDA UDI
Device Name
ADVANTIM® TIBIAL STEM 6" X 10mm LG-XL FINNED FDA UDI
Model / Reference
18700470 FDA UDI
Description
ADVANTIM® TIBIAL STEM 6" X 10mm LG-XL FINNED FDA UDI

Identifiers

Catalog Number
18700470 FDA UDI
Primary DI / UDI-DI
M684187004701 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Knee femur stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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
Length — 6 Inch FDA UDI

Category: Knee femur stem prosthesis

Advantim by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee femur stem prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a4b37920-77cc-428c-b1ed-c5c89818772b 36 fields · synced Jun 9, 2026