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RIN-11-11, Component One

FDA UDI

Class I (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
RIN-11-11, Component One FDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
Ranfac Injection Needle, F/G, Sterile P/N 74343-01M FDA UDI
Model / Reference
11 Gauge x 11cm FDA UDI
Description
Ranfac Injection Needle, F/G, Sterile P/N 74343-01M FDA UDI

Identifiers

Catalog Number
RIN-11-11 FDA UDI
Primary DI / UDI-DI
00857878007842 FDA UDI
FDA Product Code
FGY FDA UDI
GMDN Term
Bone access cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

Yes

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: Bone access cannula

RIN-11-11, Component One by Ranfac Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone access cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ranfac Corp.

Sources (1)

  • FDA UDI 63034f71-8c07-4588-98f8-36f49e805ea5 36 fields · synced May 30, 2026