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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
Tonsil snare FDA UDI
Device Name
SAGE TONSIL SNARE 9 FDA UDI
Model / Reference
55-0505 FDA UDI
Description
SAGE TONSIL SNARE 9 FDA UDI

Identifiers

Primary DI / UDI-DI
00810123202065 FDA UDI
FDA Product Code
KBZ FDA UDI
GMDN Term
Tonsil snare 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: Tonsil snare

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

Similar devices

Also classified as Tonsil snare.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Adler, Inc.

Sources (1)

  • FDA UDI 7619f0af-a47f-4291-8acc-337f734cd65d 34 fields · synced May 31, 2026