← Back to catalogue

Ambler Value Line

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Value Line FDA UDI
Generic Name
Otologic clamp FDA UDI
Device Name
Jansen-Middleton nasal septum forceps, 7 3/4'', working length 130mm, double-action, small pattern, 3.0mm x 13.0mm thru-cutting jaws, spring handle FDA UDI
Model / Reference
Jansen-Middleton nasal septum forceps FDA UDI
Description
Jansen-Middleton nasal septum forceps, 7 3/4'', working length 130mm, double-action, small pattern, 3.0mm x 13.0mm thru-cutting jaws, spring handle FDA UDI

Identifiers

Catalog Number
131-305 FDA UDI
Primary DI / UDI-DI
00190660204372 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 Value Line 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 c61dc41f-9e99-4171-9e39-2229b993fffd 35 fields · synced Jun 8, 2026