← Back to catalogue

Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Ophthalmic surgical irrigation/infusion/aspiration handle, reusable FDA UDI
Device Name
McIntyre handpiece for aspirating or irrigating, 3'' length, Luer connector and narrow tubing connector, autoclavable white plastic FDA UDI
Model / Reference
McIntyre handpiece for aspirating or irrigating FDA UDI
Description
McIntyre handpiece for aspirating or irrigating, 3'' length, Luer connector and narrow tubing connector, autoclavable white plastic FDA UDI

Identifiers

Catalog Number
6792E FDA UDI
Primary DI / UDI-DI
00190660083038 FDA UDI
FDA Product Code
KYG FDA UDI
GMDN Term
Ophthalmic surgical irrigation/infusion/aspiration handle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4360 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

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

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: Ophthalmic surgical irrigation/infusion/aspiration handle, reusable

Ambler Surgical by Ambler Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical irrigation/infusion/aspiration handle, 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

Sources (1)

  • FDA UDI e1da0657-59e8-486d-87f0-c2555757d26d 35 fields · synced May 31, 2026