← 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
Otologic clamp FDA UDI
Device Name
Greven ear forceps, 5 1/4'', working length 73.0mm, 5.0mm jaws, 2.5mm of tips serrated and touching, opening behind tip, ring handle FDA UDI
Model / Reference
Greven ear forceps FDA UDI
Description
Greven ear forceps, 5 1/4'', working length 73.0mm, 5.0mm jaws, 2.5mm of tips serrated and touching, opening behind tip, ring handle FDA UDI

Identifiers

Catalog Number
30-685 FDA UDI
Primary DI / UDI-DI
00190660054939 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Otologic clamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: Otologic clamp

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

Similar devices

Also classified as Otologic clamp.

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

Manufacturer
Ambler Surgical, LLC

Sources (1)

  • FDA UDI 51dc712a-3638-4eaf-b53f-4093fd6e788d 35 fields · synced May 31, 2026