Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name: Ambler Surgical FDA UDI
Generic Name: Nerve/vessel retractor FDA UDI
Device Name: Meyerding retractor, 7 1/2'', 2 3/8'' x 1'' wide blades, with teeth, ring handle with ratchet FDA UDI
Model / Reference: Meyerding retractor FDA UDI
Description: Meyerding retractor, 7 1/2'', 2 3/8'' x 1'' wide blades, with teeth, ring handle with ratchet FDA UDI

Identifiers

Catalog Number: 72-523 FDA UDI
Primary DI / UDI-DI: 00190660139810 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Nerve/vessel retractor FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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: Nerve/vessel retractor

Ambler Surgical 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 28146381-db3b-4a5a-a7b1-3d8fda640662 35 fields · synced May 31, 2026