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Imhs

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
IMHS FDA UDI
Generic Name
Bone nail trial, reusable FDA UDI
Device Name
IMHS CP 10MM SHORT TRIAL LEFT FDA UDI
Model / Reference
71687008 FDA UDI
Description
IMHS CP 10MM SHORT TRIAL LEFT FDA UDI

Identifiers

Catalog Number
71687008 FDA UDI
Primary DI / UDI-DI
03596010519160 FDA UDI
510(k) Number
K122170 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Bone nail trial, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone nail trial, reusable

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

Similar devices

Also classified as Bone nail trial, reusable.

Cleared under the same submission

K122170 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 6918a176-03bf-4062-a4a8-b2857c1fed1d 36 fields · synced Jun 8, 2026