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Sorbie Questor

FDA UDI

Class II (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
SORBIE QUESTOR FDA UDI
Generic Name
Hinged total elbow prosthesis FDA UDI
Model / Reference
822SMLT FDA UDI

Identifiers

Catalog Number
822SMLT FDA UDI
Primary DI / UDI-DI
00840420129314 FDA UDI
FDA Product Code
JDB FDA UDI
GMDN Term
Hinged total elbow prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3160 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

Category: Hinged total elbow prosthesis

Sorbie Questor by Wright Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hinged total elbow prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI db9fd69a-c675-45ab-b330-d79fbcee80b7 35 fields · synced Jun 8, 2026