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Resource

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
RESOURCE FDA UDI
Generic Name
Wire-extracting pliers FDA UDI
Device Name
MG WIRE CT PLIERS HW-2.5MM SW-3.5MM165MM FDA UDI
Model / Reference
LX163ZR FDA UDI
Description
MG WIRE CT PLIERS HW-2.5MM SW-3.5MM165MM FDA UDI

Identifiers

Catalog Number
LX163ZR FDA UDI
Primary DI / UDI-DI
04046955210145 FDA UDI
FDA Product Code
HTC FDA UDI
HTD FDA UDI
GMDN Term
Wire-extracting pliers 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: Wire-extracting pliers

Resource by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire-extracting pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 793ff166-a2a8-4c54-a344-64877637cb31 35 fields · synced May 30, 2026