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Cup Grasper

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
Cup Grasper FDA UDI
Generic Name
Dressing/utility forceps, scissors-like, reusable FDA UDI
Device Name
Cup Grasper, Semi Flexible, 3.0 x 260mm FDA UDI
Model / Reference
259-330-026 FDA UDI
Description
Cup Grasper, Semi Flexible, 3.0 x 260mm FDA UDI

Identifiers

Primary DI / UDI-DI
04049197514811 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Dressing/utility forceps, scissors-like, reusable 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: Dressing/utility forceps, scissors-like, reusable

Cup Grasper by RZ-Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing/utility forceps, scissors-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
RZ-Medizintechnik GmbH

Sources (1)

  • FDA UDI 64e15b90-5d4c-4aee-8b9d-f5eb565362b9 33 fields · synced Jun 8, 2026