← Back to catalogue

Cleaning Wire - Double

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name
CLEANING WIRE - DOUBLE FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI
Model / Reference
10-6171 FDA UDI

Identifiers

Primary DI / UDI-DI
D9281061710 FDA UDI
FDA Product Code
DYN FDA UDI
GMDN Term
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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: Surgical instrument/endoscope cleaning utensil, reusable

Cleaning Wire - Double by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/endoscope cleaning utensil, reusable.

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

Manufacturer
W.H. Holden, Inc.

Sources (1)

  • FDA UDI edacc74c-8231-4fed-ad76-47de0077d84f 32 fields · synced Jun 1, 2026