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Asnis

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Asnis FDA UDI
Generic Name
Bone tap, single-use FDA UDI
Device Name
CANNULATED TAP FDA UDI
Model / Reference
45-30006S FDA UDI
Description
CANNULATED TAP FDA UDI

Identifiers

Catalog Number
45-30006S FDA UDI
Primary DI / UDI-DI
04546540534224 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Bone tap, single-use 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

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

Dimensions & Sizes

Size
Length — 80.0 Millimeter FDA UDI

Category: Bone tap, single-use

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

Similar devices

Also classified as Bone tap, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI ba74d86f-cbec-4425-8030-daf5ae7aefe9 35 fields · synced May 30, 2026