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Mc-Ran-11csts

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 74402-01MModel RAN

by Ranfac Corp.

Identity

Trade Name
MC-RAN-11CSTS EUDAMED
MC-RAN-11CSTS, STERILE F/G CE FDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
Ranfac Bone Marrow Aspiration Needle EUDAMED
MC-RAN-11CSTS, STERILE F/G, CE MARROW CELLUTIONS ASPIRATION NEEDLE PN 74402-01M FDA UDI
Model / Reference
RAN EUDAMED
74402-01M EUDAMED
11 Gauge x 11CM FDA UDI
Description
MC-RAN-11CSTS, STERILE F/G, CE MARROW CELLUTIONS ASPIRATION NEEDLE PN 74402-01M FDA UDI

Identifiers

Catalog Number
MC-RAN-11CSTS FDA UDI
Primary DI / UDI-DI
00850023741516 EUDAMEDFDA UDI
Basic UDI-DI
08586900068300101G5 EUDAMED
Direct Marketing DI
00850023741516 EUDAMED
510(k) Number
K150563 FDA UDI
FDA Product Code
KNW FDA UDI
EMDN Code
A01020102 ASPIRATION FINE NEEDLES AND KITS EUDAMED
GMDN Term
Bone access cannula FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Dimensions & Sizes

Size
Needle Gauge — 11 Gauge FDA UDI
Length — 11 Centimeter FDA UDI

Category: Diskectomy system, percutaneous, automatic

Mc-Ran-11csts by Ranfac Corp. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diskectomy system, percutaneous, automatic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ranfac Corp.
EUDAMED SRN
US-MF-000008871
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED a3edcd25-5fbf-4efc-a191-ea0f6df33006 61 fields · synced Jul 15, 2026
  • FDA UDI baa62a4d-1dd1-4df9-b888-6079f4052d85 38 fields · synced May 30, 2026