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Intertan

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
INTERTAN FDA UDI
Generic Name
Femur intramedullary nail FDA UDI
Device Name
INTERTAN 11.5MM X 24CM 130D FDA UDI
Model / Reference
71934482 FDA UDI
Description
INTERTAN 11.5MM X 24CM 130D FDA UDI

Identifiers

Catalog Number
71934482 FDA UDI
Primary DI / UDI-DI
00885556105245 FDA UDI
510(k) Number
K040212 FDA UDI
K210980 FDA UDI
FDA Product Code
JDS FDA UDI
GMDN Term
Femur intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Femur intramedullary nail

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

Similar devices

Also classified as Femur intramedullary nail.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 32e8acbc-7d12-4122-9d54-5fbb56b42089 36 fields · synced Jun 8, 2026