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Adler Instrument Company

FDA UDI

Class I (US FDA UDI)

by Adler, Inc.

Identity

Trade Name
Adler Instrument Company FDA UDI
Generic Name
Nasal septum straightening forceps FDA UDI
Device Name
Jansen Middleton Septum Forceps FDA UDI
Model / Reference
50-5150 FDA UDI
Description
Jansen Middleton Septum Forceps FDA UDI

Identifiers

Primary DI / UDI-DI
00810123206261 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Nasal septum straightening forceps 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: Nasal septum straightening forceps

Adler Instrument Company by Adler, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal septum straightening forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Adler, Inc.

Sources (1)

  • FDA UDI eee700e3-b9da-4ccc-b084-5d05250a7f4c 34 fields · synced Jun 8, 2026