Ambler Value Line

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name: Ambler Value Line FDA UDI
Generic Name: Orbital depressor, reusable FDA UDI
Device Name: Knapp lacrimal sac retractor, 5 1/2'', rigid shaft, 4 sharp prongs, 6.0mm wide, flat handle FDA UDI
Model / Reference: Knapp lacrimal sac retractor FDA UDI
Description: Knapp lacrimal sac retractor, 5 1/2'', rigid shaft, 4 sharp prongs, 6.0mm wide, flat handle FDA UDI

Identifiers

Catalog Number: 72-336 FDA UDI
Primary DI / UDI-DI: 00190660208653 FDA UDI
FDA Product Code: HNI FDA UDI
GMDN Term: Orbital depressor, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orbital depressor, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Ambler Surgical, LLC

Sources (1)

FDA UDI 195127e8-c4df-4650-aa1e-c11532f6c9c1 35 fields · synced May 31, 2026