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2.70 Guide Wire Thd SS 450mm

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
2.70 Guide Wire Thd SS 450mm FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
2.70 Stainless Steel Guide Wire Threaded Tip 450mm long FDA UDI
Model / Reference
2004-0029 FDA UDI
Description
2.70 Stainless Steel Guide Wire Threaded Tip 450mm long FDA UDI

Identifiers

Catalog Number
2004-0029 FDA UDI
Primary DI / UDI-DI
00810074300391 FDA UDI
510(k) Number
K170021 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic guidewire, 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

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

No

FDA UDI

Lot / Batch Number

No

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

Dimensions & Sizes

Size
Guidewire Diameter — 2.7 Millimeter FDA UDI
Guidewire Length — 450 Millimeter FDA UDI

Category: Orthopaedic guidewire, single-use

2.70 Guide Wire Thd SS 450mm by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ea25ac14-7301-4b7d-bf4a-93a6777d746e 37 fields · synced May 31, 2026