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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 knife, single-use FDA UDI
Device Name
Miniature curved tip 1 side sharp blade, screw-in, sterile, disposable, box of 12 FDA UDI
Model / Reference
Miniature curved tip 1 side sharp blade FDA UDI
Description
Miniature curved tip 1 side sharp blade, screw-in, sterile, disposable, box of 12 FDA UDI

Identifiers

Catalog Number
6700 FDA UDI
Primary DI / UDI-DI
10190660197831 FDA UDI
FDA Product Code
HNN FDA UDI
GMDN Term
Ophthalmic knife, 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 knife, 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 knife, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4c22912f-6000-4a4d-9fd8-d5174f4882bd 35 fields · synced May 30, 2026