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Hydro-Surg

FDA UDI

Class II (US FDA UDI)

by Davol Inc.

Identity

Trade Name
Hydro-Surg FDA UDI
Generic Name
Surgical irrigation/aspiration Y-piece connector FDA UDI
Device Name
Dual Spike Adapter FDA UDI
Model / Reference
0026110 FDA UDI
Description
Dual Spike Adapter FDA UDI

Identifiers

Catalog Number
0026110 FDA UDI
Primary DI / UDI-DI
00801741010200 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical irrigation/aspiration Y-piece connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 8 Inch FDA UDI

Category: Surgical irrigation/aspiration Y-piece connector

Hydro-Surg by Davol Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration Y-piece connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI 697de85c-38b4-424e-9c8d-4c2d5bebdac1 37 fields · synced May 30, 2026