← Back to catalogue

Rbn-86

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 74049-07MModel Ranfac Marrow Biopsy Needle

by Ranfac Corp.

Identity

Trade Name
RBN-86 EUDAMED
RBN-86, F/G FDA UDI
Generic Name
Bone marrow biopsy needle, single-use FDA UDI
Device Name
RBN-84 EUDAMED
RBN-86, F/G, STERILE PN 74049-07M FDA UDI
Model / Reference
Ranfac Marrow Biopsy Needle EUDAMED
74049-07M EUDAMED
8 Gauge x 6" FDA UDI
Description
RBN-86, F/G, STERILE PN 74049-07M FDA UDI

Identifiers

Catalog Number
RBN-86 FDA UDI
Primary DI / UDI-DI
00858690006563 EUDAMEDFDA UDI
Basic UDI-DI
08586900068300701H3 EUDAMED
Direct Marketing DI
00858690006563 EUDAMED
510(k) Number
K983187 FDA UDI
FDA Product Code
KNW FDA UDI
EMDN Code
A01020299 NEEDLES AND KITS - BONE MARROW BIOPSY - OTHER EUDAMED
GMDN Term
Bone marrow biopsy needle, single-use 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 — 8 Gauge FDA UDI
Length — 6 Inch FDA UDI

Rbn-86 by Ranfac Corp. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED a33c46c9-daf2-40e5-8be1-829e5bcb6796 61 fields · synced Jul 14, 2026
  • FDA UDI f6a50ef3-33f9-4203-982a-4173e13e547b 37 fields · synced May 30, 2026