← Back to catalogue

Oper Cholangiography Catheter

FDA UDI

Class I (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
OPER CHOLANGIOGRAPHY CATHETER FDA UDI
Generic Name
Rigid endoscopic cannula, single-use FDA UDI
Device Name
OPER CHOLANGIOGRAPHY CATHETER ORC TYPE B PN 68010-01M FDA UDI
Model / Reference
18 GAUGE X 7" FDA UDI
Description
OPER CHOLANGIOGRAPHY CATHETER ORC TYPE B PN 68010-01M FDA UDI

Identifiers

Catalog Number
ORC-B FDA UDI
Primary DI / UDI-DI
00858690006310 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

Oper 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Ranfac Corp.

Sources (1)

  • FDA UDI 193177e3-b993-40a8-9c36-8f7a4da3a1e9 36 fields · synced Jun 1, 2026