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Anthology

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Anthology FDA UDI
Generic Name
Orthopaedic broach FDA UDI
Device Name
MODIFIED ANTHOLOGY BROACH SIZE 1 FDA UDI
Model / Reference
E0014803-1 FDA UDI
Description
MODIFIED ANTHOLOGY BROACH SIZE 1 FDA UDI

Identifiers

Catalog Number
E0014803-1 FDA UDI
Primary DI / UDI-DI
00885556634837 FDA UDI
510(k) Number
K123598 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Orthopaedic broach FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
Commercial Distribution
Not 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

Anthology by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K123598 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI ef152c38-b46b-4e8c-95a1-843afe42d3dd 37 fields · synced Jun 8, 2026