← Back to catalogue

Ndl, Rbn-132

FDA UDIEUDAMED

Class II (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
NDL, RBN-132 FDA UDI
Generic Name
Bone marrow biopsy needle, single-use FDA UDI
Device Name
NDL, RBN-132, STERILE, F/G FDA UDI
Model / Reference
13 GAUGE x 2" FDA UDI
Description
NDL, RBN-132, STERILE, F/G FDA UDI

Identifiers

Catalog Number
RBN-132 FDA UDI
Primary DI / UDI-DI
M9797405005M0 FDA UDI
510(k) Number
K983187 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone marrow biopsy needle, single-use 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

No

FDA UDI

Contains Latex

No

FDA UDI

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 — 13 Gauge FDA UDI
Length — 2 Inch FDA UDI

Category: Bone marrow biopsy needle, single-use

Ndl, Rbn-132 by Ranfac Corp. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy needle, single-use.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Ranfac Corp.

Sources (2)

  • FDA UDI 735226f4-c0c9-4b8b-896c-7fbb32dd979e 37 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026