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Sialography Unit Endport, 30ga

FDA UDI

Class I (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
SIALOGRAPHY UNIT ENDPORT, 30GA FDA UDI
Generic Name
Salivary gland catheter FDA UDI
Device Name
SIALOGRAPHY UNIT ENDPORT, 30GA 30G-END PN 68008-03M FDA UDI
Model / Reference
30 Gauge FDA UDI
Description
SIALOGRAPHY UNIT ENDPORT, 30GA 30G-END PN 68008-03M FDA UDI

Identifiers

Catalog Number
30G-END FDA UDI
Primary DI / UDI-DI
M9796800803M0 FDA UDI
FDA Product Code
GCB FDA UDI
GMDN Term
Salivary gland catheter 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 — 30 Gauge FDA UDI

Category: Salivary gland catheter

Sialography Unit Endport, 30ga by Ranfac Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Salivary gland catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ranfac Corp.

Sources (1)

  • FDA UDI b727e2aa-0ac1-40bb-bcd3-d6452da3676a 36 fields · synced May 30, 2026