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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
Bone nail end-cap FDA UDI
Device Name
125° AJAX Nail, Short, Ø10mm x Length 170mm, Titanium FDA UDI
Model / Reference
TI-6086S-10-170 FDA UDI
Description
125° AJAX Nail, Short, Ø10mm x Length 170mm, Titanium FDA UDI

Identifiers

Primary DI / UDI-DI
08903993423219 FDA UDI
510(k) Number
K192003 FDA UDI
FDA Product Code
JDS FDA UDI
GMDN Term
Bone nail end-cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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: Bone nail end-cap

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

Similar devices

Also classified as Bone nail end-cap.

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 65677e1e-72fd-47fb-b404-fd47701738ba 35 fields · synced May 30, 2026