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Disc Cath

FDA UDI

Class II (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
Disc Cath FDA UDI
Generic Name
Spinal needle, single-use FDA UDI
Device Name
Disc Cath P/N: 76102-02M FDA UDI
Model / Reference
17GA X 6" FDA UDI
Description
Disc Cath P/N: 76102-02M FDA UDI

Identifiers

Catalog Number
Disc Cath FDA UDI
Primary DI / UDI-DI
00858690006242 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Spinal needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5150 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 — 6 Inch FDA UDI
Needle Gauge — 17 Gauge FDA UDI

Category: Spinal needle, single-use

Disc Cath by Ranfac Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ranfac Corp.

Sources (1)

  • FDA UDI 9bffc1a9-83d3-4b73-acb9-be15bda0e9ac 36 fields · synced Jun 1, 2026