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Walcott Rx Products

FDA UDI

Class I (US FDA UDI)

by Walcott Rx Product Inc

Identity

Trade Name
Walcott Rx Products FDA UDI
Generic Name
Surgical irrigation/aspiration handpiece, reusable FDA UDI
Device Name
Irrigating Handle FDA UDI
Model / Reference
Rx7-022-17 FDA UDI
Description
Irrigating Handle FDA UDI

Identifiers

Primary DI / UDI-DI
00840285305236 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Surgical irrigation/aspiration handpiece, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical irrigation/aspiration handpiece, reusable

Walcott Rx Products by Walcott Rx Product Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration handpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walcott Rx Product Inc

Sources (1)

  • FDA UDI 6acc9504-ee74-4175-8a0e-d7e3ecb9ed15 34 fields · synced May 31, 2026