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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
Dressing/utility forceps, scissors-like, reusable FDA UDI
Device Name
Hunter fenestrated debakey grasping forceps, 3-piece take apart, rotatable, double-action, 5.0mm diameter, 450.0mm working length, insulated shaft, 20.0mm straight jaws, carbon fiber ring handle with ratchet catch FDA UDI
Model / Reference
Hunter fenestrated debakey grasping forceps FDA UDI
Description
Hunter fenestrated debakey grasping forceps, 3-piece take apart, rotatable, double-action, 5.0mm diameter, 450.0mm working length, insulated shaft, 20.0mm straight jaws, carbon fiber ring handle with ratchet catch FDA UDI

Identifiers

Catalog Number
97-047 FDA UDI
Primary DI / UDI-DI
00190660204280 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Dressing/utility forceps, scissors-like, reusable 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dressing/utility forceps, scissors-like, reusable

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

Similar devices

Also classified as Dressing/utility forceps, scissors-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4b12dbe9-8f9c-465c-90ff-286c87528647 35 fields · synced Jun 6, 2026