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Novo Surgical Inc.

FDA UDI

Class I (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name
Novo Surgical Inc. FDA UDI
Generic Name
Adenoid curette, reusable FDA UDI
Device Name
meltzer adenoid punch, triangular basket, shaft 120.0 mm, overall 7 3/4" (19.5 cm), 6.0 mm bite, 7.0 mm basket FDA UDI
Model / Reference
E8263-32 FDA UDI
Description
meltzer adenoid punch, triangular basket, shaft 120.0 mm, overall 7 3/4" (19.5 cm), 6.0 mm bite, 7.0 mm basket FDA UDI

Identifiers

Primary DI / UDI-DI
00842331194429 FDA UDI
FDA Product Code
KBS FDA UDI
GMDN Term
Adenoid curette, reusable 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: Adenoid curette, reusable

Novo Surgical Inc. by Novo Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Adenoid curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novo Surgical, Inc.

Sources (1)

  • FDA UDI 38d441b2-8455-4e3b-96cb-f1c030e28db8 34 fields · synced May 30, 2026