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Bone Access Needle

FDA UDIEUDAMED

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Bone Access Needle FDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
Bone Access Needle 8ga x 6in FDA UDI
Model / Reference
DBANJ0806TL FDA UDI
Description
Bone Access Needle 8ga x 6in FDA UDI

Identifiers

Catalog Number
DBANJ0806TL FDA UDI
Primary DI / UDI-DI
00886333227112 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone access cannula FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bone access cannula

Bone Access Needle by Argon Medical Devices, Inc. — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone access cannula.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 0081b1fb-0386-4c0b-be9e-4dead25936c0 37 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026