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Confidence Spinal Cement System

FDA UDI

Class I (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
CONFIDENCE SPINAL CEMENT SYSTEM FDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
CONFIDENCE SPINAL CEMENT SYSTEM INTRODUCER NEEDLE, SIDE HOLE 13G x 6 Inches FDA UDI
Model / Reference
283904613 FDA UDI
Description
CONFIDENCE SPINAL CEMENT SYSTEM INTRODUCER NEEDLE, SIDE HOLE 13G x 6 Inches FDA UDI

Identifiers

Catalog Number
283904613 FDA UDI
Primary DI / UDI-DI
10705034209548 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Bone access cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Category: Bone access cannula

Confidence Spinal Cement System by Medos International Sàrl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone access cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 33904521-327b-4c0a-9d9b-6699b8295f7e 35 fields · synced Jun 1, 2026