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Airlockna

FDA UDI

Class I (US FDA UDI)

by Novastep

Identity

Trade Name
AIRLOCKNA FDA UDI
Generic Name
Orthopaedic intraoperative positioning pin, single-use FDA UDI
Device Name
Threaded K-wire Ø2.5 - Opening Wedge distractor FDA UDI
Model / Reference
CKW04001 FDA UDI
Description
Threaded K-wire Ø2.5 - Opening Wedge distractor FDA UDI

Identifiers

Catalog Number
CKW04001 FDA UDI
Primary DI / UDI-DI
03700879512884 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Orthopaedic intraoperative positioning pin, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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 intraoperative positioning pin, single-use

Airlockna by Novastep — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic intraoperative positioning pin, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novastep

Sources (1)

  • FDA UDI 8306b87e-ae1b-4703-b296-15cf556e3a2e 35 fields · synced May 30, 2026