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AJAX Nail

FDA UDI

Class II (US FDA UDI)

by Auxein Medical Private Limited

Identity

Trade Name
AJAX Nail FDA UDI
Generic Name
Tibia intramedullary nail FDA UDI
Device Name
AJAX 4.9mm Locking Bolt, Self Tapping, Length 50mm, Titanium FDA UDI
Model / Reference
TI-6085-01-050 FDA UDI
Description
AJAX 4.9mm Locking Bolt, Self Tapping, Length 50mm, Titanium FDA UDI

Identifiers

Primary DI / UDI-DI
08903993396773 FDA UDI
510(k) Number
K192003 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Tibia intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Tibia intramedullary nail

AJAX Nail by Auxein Medical Private Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tibia intramedullary nail.

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 62916cdf-5f2c-4a2c-860a-e625a896fb70 35 fields · synced May 30, 2026