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Asnis

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
ASNIS FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Cannulated Screw FDA UDI
Model / Reference
602910S FDA UDI
Description
Cannulated Screw FDA UDI

Identifiers

Catalog Number
602910S FDA UDI
Primary DI / UDI-DI
04546540088284 FDA UDI
FDA Product Code
HWC FDA UDI
HTN FDA UDI
OUR FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
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

Dimensions & Sizes

Size
Length — 110.0 Millimeter FDA UDI

Category: Orthopaedic bone screw (non-sliding)

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

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 5e944b3d-dc22-495f-9d65-88e8f3a414b9 35 fields · synced May 31, 2026