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Asnis

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
ASNIS FDA UDI
Generic Name
Orthopaedic guidewire, reusable FDA UDI
Device Name
Positioning Guide JFX FDA UDI
Model / Reference
705371 FDA UDI
Description
Positioning Guide JFX FDA UDI

Identifiers

Catalog Number
705371 FDA UDI
Primary DI / UDI-DI
07613327172812 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic guidewire, 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

Category: Orthopaedic guidewire, reusable

Asnis by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 0d7f4d9d-8d63-43bb-80ca-6a74f51e84b4 34 fields · synced May 30, 2026