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Anatomical Shoulder™

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Anatomical Shoulder™ FDA UDI
Generic Name
Medullary canal orthopaedic reamer, rigid FDA UDI
Device Name
AS FX RASP EXTENSION 14.5 FDA UDI
Model / Reference
01.04237.146 FDA UDI
Description
AS FX RASP EXTENSION 14.5 FDA UDI

Identifiers

Catalog Number
01.04237.146 FDA UDI
Primary DI / UDI-DI
00889024287112 FDA UDI
510(k) Number
K103404 FDA UDI
K142403 FDA UDI
FDA Product Code
KWS FDA UDI
KWT FDA UDI
HSD FDA UDI
PHX FDA UDI
GMDN Term
Medullary canal orthopaedic reamer, rigid FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3650 FDA UDI
888.3690 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Medullary canal orthopaedic reamer, rigid

Anatomical Shoulder™ by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medullary canal orthopaedic reamer, rigid.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI e95d4add-e033-4af3-89e9-abc204232843 36 fields · synced Jun 6, 2026