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Peri-Loc

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Peri-Loc FDA UDI
Generic Name
Internal orthopaedic fixation system, cerclage wire/cable, sterile FDA UDI
Device Name
PERI-LOC TGR K-WIRE 2.0MM X 350MM FDA UDI
Model / Reference
71173381 FDA UDI
Description
PERI-LOC TGR K-WIRE 2.0MM X 350MM FDA UDI

Identifiers

Catalog Number
71173381 FDA UDI
Primary DI / UDI-DI
03596010538505 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Internal orthopaedic fixation system, cerclage wire/cable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Internal orthopaedic fixation system, cerclage wire/cable, sterile

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

Similar devices

Also classified as Internal orthopaedic fixation system, cerclage wire/cable, sterile.

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 138104fb-141f-4747-b4a1-85b467d94405 35 fields · synced Jun 8, 2026