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Acufex

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
ACUFEX FDA UDI
Generic Name
Bone tunnel plug, non-cannulated FDA UDI
Device Name
5 - 6 MM BONE TUNNEL PLUG FDA UDI
Model / Reference
72201735 FDA UDI
Description
5 - 6 MM BONE TUNNEL PLUG FDA UDI

Identifiers

Catalog Number
72201735 FDA UDI
Primary DI / UDI-DI
23596010607090 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Bone tunnel plug, non-cannulated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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

Yes

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

Category: Bone tunnel plug, non-cannulated

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

Similar devices

Also classified as Bone tunnel plug, non-cannulated.

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 8fcde398-7bed-4d8d-8bae-6e73ee40554b 35 fields · synced Jun 8, 2026