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Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
Retrobulbar anesthesia needle, 25 gauge x 1'', straight, packaged individually, sterile, disposable, box of 10 * * SPECIAL ORDER PRODUCT - MINIMUM ORDER OF 20 BOXES AND 4-6 WEEK LEAD TIME * * FDA UDI
Model / Reference
Retrobulbar anesthesia needle FDA UDI
Description
Retrobulbar anesthesia needle, 25 gauge x 1'', straight, packaged individually, sterile, disposable, box of 10 * * SPECIAL ORDER PRODUCT - MINIMUM ORDER OF 20 BOXES AND 4-6 WEEK LEAD TIME * * FDA UDI

Identifiers

Catalog Number
111278 FDA UDI
Primary DI / UDI-DI
10190660198371 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

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

Similar devices

Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 78db9cf3-6781-4221-b3be-3896cdb2f3ac 35 fields · synced Jun 6, 2026