← Back to catalogue

Pusher, for Valve positioning 35cm

FDA UDI

Class I (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name
Pusher, for Valve positioning 35cm FDA UDI
Generic Name
Suture knot pusher, reusable FDA UDI
Device Name
Pusher, for Valve positioning 35cm ValveGate™ FDA UDI
Model / Reference
34-7465 FDA UDI
Description
Pusher, for Valve positioning 35cm ValveGate™ FDA UDI

Identifiers

Catalog Number
34-7465 FDA UDI
Primary DI / UDI-DI
04057034120552 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Suture knot pusher, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suture knot pusher, reusable

Pusher, for Valve positioning 35cm by Geister Medizin Technik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suture knot pusher, reusable.

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

Sources (1)

  • FDA UDI ad6a3d9b-c0f5-45be-ab3d-a4581b02b218 35 fields · synced Jun 6, 2026