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Ascend™

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
Ascend™ FDA UDI
Generic Name
Coated shoulder humeral stem prosthesis FDA UDI
Model / Reference
502448 FDA UDI

Identifiers

Catalog Number
502448 FDA UDI
Primary DI / UDI-DI
00846832004324 FDA UDI
FDA Product Code
KWT FDA UDI
KWS FDA UDI
HSD FDA UDI
GMDN Term
Coated shoulder humeral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3650 FDA UDI
888.3660 FDA UDI
888.3690 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 48 Millimeter FDA UDI

Ascend™ by Tornier, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI dad3bba4-cd4e-47f1-afdc-5057639bb697 36 fields · synced May 31, 2026