← Back to catalogue

Spec Irrig Tip - Centerfor

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name
SPEC IRRIG TIP - CENTERFOR FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, illuminating, reusable FDA UDI
Model / Reference
83-8111 FDA UDI

Identifiers

Primary DI / UDI-DI
D9288381110 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Surgical irrigation/aspiration cannula, illuminating, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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 irrigation/aspiration cannula, illuminating, reusable

Spec Irrig Tip - Centerfor by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration cannula, illuminating, 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 b796d227-28f1-4004-9e01-0de979166fd6 32 fields · synced May 29, 2026