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Ran-132

FDA UDI

Class II (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
RAN-132 FDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
NEEDLE, RAN-132, F/G, STERILE, RANFAC P/N 74415-01M FDA UDI
Model / Reference
13 GA X 2 IN FDA UDI
Description
NEEDLE, RAN-132, F/G, STERILE, RANFAC P/N 74415-01M FDA UDI

Identifiers

Catalog Number
RAN-132 FDA UDI
Primary DI / UDI-DI
00850023741745 FDA UDI
510(k) Number
K131157 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone access cannula 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
Length — 2 Inch FDA UDI
Needle Gauge — 13 Gauge FDA UDI

Category: Bone access cannula

Ran-132 by Ranfac Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone access cannula.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ranfac Corp.

Sources (1)

  • FDA UDI 1865e888-e3db-4d0c-9b55-257979adac6f 37 fields · synced Jun 8, 2026