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Pistol Guidewire Gripper

FDA UDI

Class I (US FDA UDI)

by Tecomet, Inc

Identity

Trade Name
Pistol Guidewire Gripper FDA UDI
Generic Name
Orthopaedic implantation sleeve, reusable FDA UDI
Device Name
Guide Wire Holder, Pistol Grip FDA UDI
Model / Reference
2810-01-001 FDA UDI
Description
Guide Wire Holder, Pistol Grip FDA UDI

Identifiers

Primary DI / UDI-DI
00841435119833 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Orthopaedic implantation sleeve, reusable 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implantation sleeve, reusable

Pistol Guidewire Gripper by Tecomet, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantation sleeve, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tecomet, Inc

Sources (1)

  • FDA UDI fbff2da3-0d91-47e8-8591-77ce099e8929 33 fields · synced Sep 18, 2026