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Ran-811-Ct

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 74276-05MModel RAN

by Ranfac Corp.

Identity

Trade Name
RAN-811-CT EUDAMEDFDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
Ranfac Bone Marrow Aspiration Needle EUDAMED
RAN-811-CT P/N 74276-05M FDA UDI
Model / Reference
RAN EUDAMED
74276-05M EUDAMED
8 GAUGE X 11CM FDA UDI
Description
RAN-811-CT P/N 74276-05M FDA UDI

Identifiers

Catalog Number
RAN-811-CT FDA UDI
Primary DI / UDI-DI
00857878007385 EUDAMEDFDA UDI
Basic UDI-DI
08586900068300101G5 EUDAMED
Direct Marketing DI
00857878007385 EUDAMED
510(k) Number
K131157 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
Length — 11 Centimeter FDA UDI
Needle Gauge — 8 Gauge FDA UDI

Category: Diskectomy system, percutaneous, automatic

Ran-811-Ct 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 a9538b28-82fb-400c-976a-50fd487bce27 61 fields · synced Jul 18, 2026
  • FDA UDI 2fcb402e-5fd9-4f1f-86d4-0f62d1ae086b 37 fields · synced May 30, 2026