Bone Access Kit

FDA UDI

Class I (US FDA UDI)

by Custom Interventional Pain Management

Identity

Trade Name: Bone Access Kit FDA UDI
Generic Name: Bone marrow biopsy procedure kit FDA UDI
Device Name: Convenience kit with Lidocaine FDA UDI
Model / Reference: TRAP FDA UDI
Description: Convenience kit with Lidocaine FDA UDI

Identifiers

Catalog Number: TRAP FDA UDI
Primary DI / UDI-DI: B875TRAPLID0 FDA UDI
FDA Product Code: PXO FDA UDI
GMDN Term: Bone marrow biopsy procedure kit 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Bone marrow biopsy procedure kit

Bone Access Kit by Custom Interventional Pain Management — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Custom Interventional Pain Management

Sources (1)

FDA UDI 0447fe6f-c274-4692-9637-9bda20cf2c52 34 fields · synced Jun 8, 2026