Mielo-Can Iliac

FDA UDI

Class II (US FDA UDI)

by Sterylab Srl

Identity

Trade Name: MIELO-CAN ILIAC FDA UDI
Generic Name: Bone marrow biopsy procedure kit FDA UDI
Device Name: Iliac crest bone-marrow explantation needle 14G; 8 cm FDA UDI
Model / Reference: MIELO-CAN ILIAC FDA UDI
Description: Iliac crest bone-marrow explantation needle 14G; 8 cm FDA UDI

Identifiers

Catalog Number: MCN04I FDA UDI
Primary DI / UDI-DI: 08033959228234 FDA UDI
510(k) Number: K051506 FDA UDI
FDA Product Code: KNW FDA UDI
FCG FDA UDI
GMDN Term: Bone marrow biopsy procedure kit 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

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

Dimensions & Sizes

Size: Needle Gauge — 14 Gauge FDA UDI

Category: Bone marrow biopsy procedure kit

Mielo-Can Iliac by Sterylab Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K051506 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Sterylab Srl

Sources (1)

FDA UDI dd0726ba-917c-479a-b908-0a08e098d18d 36 fields · synced May 30, 2026