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AccuThrive®

FDA UDI

Class I (US FDA UDI)

by AccuTec, Inc.

Identity

Trade Name
AccuThrive® FDA UDI
Generic Name
Dressing/utility forceps, scissors-like, reusable FDA UDI
Device Name
AccuThrive Scalpel Blade Applicator and Remover Forceps 16cm (1EA/CA) FDA UDI
Model / Reference
Blade Applicator and Remover Forceps FDA UDI
Description
AccuThrive Scalpel Blade Applicator and Remover Forceps 16cm (1EA/CA) FDA UDI

Identifiers

Catalog Number
AVAN-1008-0000 FDA UDI
Primary DI / UDI-DI
00843382114329 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Dressing/utility forceps, scissors-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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: Dressing/utility forceps, scissors-like, reusable

AccuThrive® by AccuTec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing/utility forceps, scissors-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AccuTec, Inc.

Sources (1)

  • FDA UDI e0d48ae0-61cc-40a3-8b41-e642ebb20475 35 fields · synced Jun 1, 2026