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Cement Injection Cannula

FDA UDI

Class I (US FDA UDI)

by Adria Srl

Identity

Trade Name
Cement Injection Cannula FDA UDI
Generic Name
Vertebral bone biopsy procedure kit, single-use FDA UDI
Device Name
Cement injection cannula FDA UDI
Model / Reference
495041420 FDA UDI
Description
Cement injection cannula FDA UDI

Identifiers

Primary DI / UDI-DI
08053175004382 FDA UDI
FDA Product Code
OAR FDA UDI
GMDN Term
Vertebral bone biopsy procedure kit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4200 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Vertebral bone biopsy procedure kit, single-use

Cement Injection Cannula by Adria Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vertebral bone biopsy procedure kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Adria Srl

Sources (1)

  • FDA UDI feb07a44-08b2-480f-b07f-e9115829f464 33 fields · synced May 30, 2026