← Back to catalogue

RZ Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
RZ Medizintechnik GmbH FDA UDI
Generic Name
Surgical gastrointestinal clamp FDA UDI
Device Name
MAYO ROBSON ATRAUMATIC Intestinal Clamp 210mm, 8 1/4'', curved atraumatic serrations FDA UDI
Model / Reference
310-141-210 FDA UDI
Description
MAYO ROBSON ATRAUMATIC Intestinal Clamp 210mm, 8 1/4'', curved atraumatic serrations FDA UDI

Identifiers

Catalog Number
310-141-210 FDA UDI
Primary DI / UDI-DI
04049197257541 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Surgical gastrointestinal clamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical gastrointestinal clamp

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

Similar devices

Also classified as Surgical gastrointestinal clamp.

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 67c3bd7d-47ee-4b19-93e4-7878cf18f9e5 35 fields · synced May 31, 2026