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Wire Twister D/E Ch Handle 4mm Deep

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name
WIRE TWISTER D/E CH HANDLE 4MM DEEP FDA UDI
Generic Name
Wire holding/twisting forceps FDA UDI
Model / Reference
20-1131CH FDA UDI

Identifiers

Primary DI / UDI-DI
D928201131CH0 FDA UDI
FDA Product Code
ECN FDA UDI
GMDN Term
Wire holding/twisting forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 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: Wire holding/twisting forceps

Wire Twister D/E Ch Handle 4mm Deep by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire holding/twisting forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W.H. Holden, Inc.

Sources (1)

  • FDA UDI dcd54328-e126-4e86-9aa8-e4bef56f1e35 32 fields · synced May 30, 2026