← Back to catalogue

Probe, Articulating

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
Probe, Articulating FDA UDI
Generic Name
Vessel approximator FDA UDI
Device Name
Probe, Articulating, 3.0 x 330mm FDA UDI
Model / Reference
259-695-001 FDA UDI
Description
Probe, Articulating, 3.0 x 330mm FDA UDI

Identifiers

Primary DI / UDI-DI
04049197517973 FDA UDI
FDA Product Code
HXB FDA UDI
GMDN Term
Vessel approximator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Vessel approximator

Probe, Articulating by RZ-Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vessel approximator.

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
RZ-Medizintechnik GmbH

Sources (1)

  • FDA UDI afc0f09c-443f-4a1a-a83a-ea9706e50ad1 33 fields · synced May 30, 2026