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AccuThrive®

FDA UDI

Class I (US FDA UDI)

by AccuTec, Inc.

Identity

Trade Name
AccuThrive® FDA UDI
Generic Name
Skin biopsy blade FDA UDI
Device Name
ACCUTHRIVE DERMABLADE BIOPSY BLADE SS STERILE USA 400BL/CA (50BL/CT, 8CT/CS) FDA UDI
Model / Reference
Biopsy Blade FDA UDI
Description
ACCUTHRIVE DERMABLADE BIOPSY BLADE SS STERILE USA 400BL/CA (50BL/CT, 8CT/CS) FDA UDI

Identifiers

Catalog Number
AVSC-1135-0000 FDA UDI
Primary DI / UDI-DI
00843382113827 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Skin biopsy blade 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin biopsy blade

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

Similar devices

Also classified as Skin biopsy blade.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AccuTec, Inc.

Sources (1)

  • FDA UDI e8b0eefd-2fbe-4bd7-afa1-54d6d8bfbd4d 35 fields · synced Jun 1, 2026