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T2

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
T2 FDA UDI
Generic Name
Humerus intramedullary nail FDA UDI
Device Name
Proximal Humeral Nail Long, RIGHT FDA UDI
Model / Reference
1832-3822S FDA UDI
Description
Proximal Humeral Nail Long, RIGHT FDA UDI

Identifiers

Catalog Number
1832-3822S FDA UDI
Primary DI / UDI-DI
04546540437136 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Humerus intramedullary nail 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

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

Dimensions & Sizes

Size
Length — 220.0 Millimeter FDA UDI

Category: Humerus intramedullary nail

T2 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Humerus intramedullary nail.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI af3474c0-dc5f-4b77-a077-ed12f8eccef1 35 fields · synced Jun 1, 2026