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In2Bones

FDA UDI

Class I (US FDA UDI)

by In2Bones, USA

Identity

Trade Name
In2Bones FDA UDI
Generic Name
Orthopaedic implantation sleeve, reusable FDA UDI
Device Name
.045 x 4.0 in. K-wire, double diamond, Non-Sterile FDA UDI
Model / Reference
C01 N0011 FDA UDI
Description
.045 x 4.0 in. K-wire, double diamond, Non-Sterile FDA UDI

Identifiers

Catalog Number
C01 N0011 FDA UDI
Primary DI / UDI-DI
00817906029581 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Orthopaedic implantation sleeve, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implantation sleeve, reusable

A comprehensive directory of medical devices, including In2Bones Orthopaedic implantation sleeve. Find detailed information about its features, compliance, and FAQs.

Similar devices

Also classified as Orthopaedic implantation sleeve, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
In2Bones, USA

Sources (1)

  • FDA UDI ce6aa8bc-cc00-4d68-b1af-b7c39a84b900 35 fields · synced Jul 15, 2026