Banran-11

FDA UDI

Class II (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name: BANRAN-11 FDA UDI
Generic Name: Bone access cannula FDA UDI
Device Name: BANRAN-11, F/G, STERILE, P/N 76153-01M FDA UDI
Model / Reference: 11GA X 4CM FDA UDI
Description: BANRAN-11, F/G, STERILE, P/N 76153-01M FDA UDI

Identifiers

Catalog Number: BANRAN-11 FDA UDI
Primary DI / UDI-DI: 00850023741967 FDA UDI
FDA Product Code: KNW FDA UDI
OCJ FDA UDI
GMDN Term: Bone access cannula FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1075 FDA UDI
888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 11 Gauge FDA UDI
Needle Gauge — 15 Gauge FDA UDI
Length — 4 Centimeter FDA UDI
Length — 4 Inch FDA UDI

Category: Bone access cannula

Banran-11 by Ranfac Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Ranfac Corp.

Sources (1)

FDA UDI 603a4621-0523-4c37-b27f-9acaa0581ceb 36 fields · synced May 30, 2026