← Back to catalogue

CANYON™ Retractor Systems

FDA UDI

Class I (US FDA UDI)

by K2m, Inc.

Identity

Trade Name
CANYON™ Retractor Systems FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Slotted Port Size Ø20x80 mm FDA UDI
Model / Reference
AN01-91518 FDA UDI
Description
Slotted Port Size Ø20x80 mm FDA UDI

Identifiers

Catalog Number
AN01-91518 FDA UDI
Primary DI / UDI-DI
10888857490345 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Dimensions & Sizes

Size
Outer Diameter — 20 Millimeter FDA UDI
Length — 80 Millimeter FDA UDI

Category: Surgical retractor/retraction system blade, reusable

CANYON™ Retractor Systems by K2m, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
K2m, Inc.

Sources (1)

  • FDA UDI 0a1ca759-92d9-49aa-a390-a6f7e1c34b1c 36 fields · synced May 30, 2026