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Vertebra Access Device wth Trocar Tip Access Needle

FDA UDI

Class II (US FDA UDI)

by Joline GmbH & Co. KG

Identity

Trade Name
Vertebra Access Device wth Trocar Tip Access Needle FDA UDI
Generic Name
Bone access cannula FDA UDI
Model / Reference
US9101 FDA UDI

Identifiers

Primary DI / UDI-DI
04250203940726 FDA UDI
510(k) Number
K192449 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Bone access cannula FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

No

FDA UDI

Category: Bone access cannula

Vertebra Access Device wth Trocar Tip Access Needle by Joline GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone access cannula.

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 1494d5ea-5d9a-4107-9c29-0e4d57140554 33 fields · synced Jun 8, 2026