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: Mueller phlebectomy hook, set of 4 includes sizes #1, #2, #3 and #4, right handed, flat handle (37-882, 37-884, 37-556 and 37-888) FDA UDI
Model / Reference: Mueller phlebectomy hook FDA UDI
Description: Mueller phlebectomy hook, set of 4 includes sizes #1, #2, #3 and #4, right handed, flat handle (37-882, 37-884, 37-556 and 37-888) FDA UDI

Identifiers

Catalog Number: 37-880 FDA UDI
Primary DI / UDI-DI: 00190660086015 FDA UDI
FDA Product Code: GDG 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

Yes

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 ef69d2a3-fa76-4617-a48c-bd3859b5b409 35 fields · synced Jun 6, 2026