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EXPert

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
EXPert FDA UDI
Generic Name
Surgical implant/trial-implant/sizer holder, reusable FDA UDI
Device Name
RADIOLUCENT INSERTION HANDLE FOR EXPERT ALFN/100MM FDA UDI
Model / Reference
03.010.488 FDA UDI
Description
RADIOLUCENT INSERTION HANDLE FOR EXPERT ALFN/100MM FDA UDI

Identifiers

Catalog Number
03010488 FDA UDI
Primary DI / UDI-DI
10886982069061 FDA UDI
510(k) Number
K070843 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Surgical implant/trial-implant/sizer holder, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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: Surgical implant/trial-implant/sizer holder, reusable

EXPert by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant/trial-implant/sizer holder, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI 509a6791-4bd8-45a1-b55f-97c34675a58a 36 fields · synced Jun 8, 2026