← Back to catalogue

Schwert

FDA UDI

Class I (US FDA UDI)

by A. Schweickhardt GmbH & Co. KG

Identity

Trade Name
SCHWERT FDA UDI
Generic Name
Wire cutter FDA UDI
Device Name
Distal cutter mini slim, 11,5 cm delicate design, HCS insert max 0,534x0,635mm/0,021x0,025 FDA UDI
Model / Reference
5226 FDA UDI
Description
Distal cutter mini slim, 11,5 cm delicate design, HCS insert max 0,534x0,635mm/0,021x0,025 FDA UDI

Identifiers

Catalog Number
5226 FDA UDI
Primary DI / UDI-DI
E89652260 FDA UDI
FDA Product Code
HXZ FDA UDI
GMDN Term
Wire cutter 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: Wire cutter

Schwert by A. Schweickhardt GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire cutter.

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 c1c18286-488c-4504-869f-8f424693872a 35 fields · synced May 30, 2026