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Princeton

FDA UDI

Class I (US FDA UDI)

by Princeton Medical Group, Inc.

Identity

Trade Name
PRINCETON FDA UDI
Generic Name
Angiographic catheter, single-use FDA UDI
Device Name
FORCEP CHOLANGIOGRAM 5.0MM 33CM DISPOSABLE STERILE BOX OF 10 FDA UDI
Model / Reference
MAS007 FDA UDI
Description
FORCEP CHOLANGIOGRAM 5.0MM 33CM DISPOSABLE STERILE BOX OF 10 FDA UDI

Identifiers

Catalog Number
MAS007 FDA UDI
Primary DI / UDI-DI
G587MAS0070 FDA UDI
FDA Product Code
GBZ FDA UDI
GMDN Term
Angiographic catheter, 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

No

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

Yes

FDA UDI

Category: Angiographic catheter, single-use

Princeton by Princeton Medical Group, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b676a1b5-fcb7-4b04-a7c5-2ea80dea3d5e 35 fields · synced Jun 1, 2026