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Affixus®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Affixus® FDA UDI
Generic Name
Tibia intramedullary nail FDA UDI
Model / Reference
815409240 FDA UDI

Identifiers

Catalog Number
815409240 FDA UDI
Primary DI / UDI-DI
00887868141966 FDA UDI
510(k) Number
K150867 FDA UDI
K241651 FDA UDI
FDA Product Code
HWC FDA UDI
HSB FDA UDI
JDS FDA UDI
GMDN Term
Tibia intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3020 FDA UDI
888.3030 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
MRI Safety
MR Conditional FDA UDI

Category: Tibia intramedullary nail

Affixus® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tibia intramedullary nail.

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 3daf3954-948a-47f4-8c1f-1d202e9457a7 36 fields · synced May 30, 2026