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6.0 X 90mm Outer Sleeve

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
6.0 X 90MM OUTER SLEEVE FDA UDI
Generic Name
Orthopaedic instrument extractor FDA UDI
Device Name
6.0 X 90MM OUTER SLEEVE FDA UDI
Model / Reference
303-6003 FDA UDI
Description
6.0 X 90MM OUTER SLEEVE FDA UDI

Identifiers

Catalog Number
303-6003 FDA UDI
Primary DI / UDI-DI
00816950029820 FDA UDI
510(k) Number
K160603 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Orthopaedic instrument extractor 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

No

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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 6.0 Millimeter FDA UDI
Length — 90 Millimeter FDA UDI

Category: Orthopaedic instrument extractor

6.0 X 90mm Outer Sleeve by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic instrument extractor.

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 47e1c4d2-755a-447b-b617-5d684395797f 37 fields · synced May 30, 2026