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Hintermann Series

FDA UDI

Class I (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
Hintermann Series FDA UDI
Generic Name
Wire-extracting pliers FDA UDI
Device Name
Hintermann Series Parallel Pliers FDA UDI
Model / Reference
HT-39600 FDA UDI
Description
Hintermann Series Parallel Pliers FDA UDI

Identifiers

Primary DI / UDI-DI
00841731142337 FDA UDI
510(k) Number
K240475 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Wire-extracting pliers 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

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

No

FDA UDI

Lot / Batch Number

No

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

Hintermann Series by Vilex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire-extracting pliers.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vilex, Inc.

Sources (1)

  • FDA UDI 8bd856ed-c68b-46e7-9dff-eb92c8669c08 36 fields · synced May 30, 2026