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Lap Cholangiography Catheter

FDA UDI

Class I (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
LAP CHOLANGIOGRAPHY CATHETER FDA UDI
Generic Name
Rigid endoscopic cannula, single-use FDA UDI
Device Name
LAP CHOLANGIOGRAPHY CATHETER LAP-13 FDA UDI
Model / Reference
18 GAUGE x 13" FDA UDI
Description
LAP CHOLANGIOGRAPHY CATHETER LAP-13 FDA UDI

Identifiers

Catalog Number
LAP-13 FDA UDI
Primary DI / UDI-DI
00858690006945 FDA UDI
FDA Product Code
GBZ FDA UDI
GMDN Term
Rigid endoscopic cannula, single-use 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

Category: Rigid endoscopic cannula, single-use

Lap Cholangiography Catheter by Ranfac Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic cannula, 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 c0936008-26f5-430b-a043-5d88f5ff16d0 36 fields · synced May 30, 2026