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Biosteon IntraLine

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Biosteon IntraLine FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
4.5MM BIOSTEON INTRALINE PUNCH TAP FDA UDI
Model / Reference
3910-002-045 FDA UDI
Description
4.5MM BIOSTEON INTRALINE PUNCH TAP FDA UDI

Identifiers

Catalog Number
3910-002-045 FDA UDI
Primary DI / UDI-DI
07613252293187 FDA UDI
FDA Product Code
HWX FDA UDI
GMDN Term
Bone tap, 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: Bone tap, reusable

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

Similar devices

Also classified as Bone tap, 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 40a8ba30-ef78-4ac3-a06c-39c0cc38bfea 36 fields · synced Jun 1, 2026