← Back to catalogue

Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Razor blade breaker/holder FDA UDI
Device Name
Tapered series ENT round stock knife handle, 4'', round handle FDA UDI
Model / Reference
Tapered series ENT round stock knife handle FDA UDI
Description
Tapered series ENT round stock knife handle, 4'', round handle FDA UDI

Identifiers

Catalog Number
38-225 FDA UDI
Primary DI / UDI-DI
00190660092627 FDA UDI
FDA Product Code
GDZ FDA UDI
GMDN Term
Razor blade breaker/holder 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: Razor blade breaker/holder

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

Similar devices

Also classified as Razor blade breaker/holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a2c7adb5-4622-427d-a6a8-09cf0fd6f121 35 fields · synced Jun 8, 2026