← Back to catalogue

CurPro Dermal Curettes, 2 mm

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
CurPro Dermal Curettes,2 mm FDA UDI
Generic Name
Epithelial cell adhesion molecule (EpCAM) IVD, antibody FDA UDI
Device Name
Sterile-R FDA UDI
Model / Reference
4155 FDA UDI
Description
Sterile-R FDA UDI

Identifiers

Primary DI / UDI-DI
00840117338463 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Epithelial cell adhesion molecule (EpCAM) IVD, antibody 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

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

Yes

FDA UDI

Category: Epithelial cell adhesion molecule (EpCAM) IVD, antibody

CurPro Dermal Curettes, 2 mm by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Epithelial cell adhesion molecule (EpCAM) IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI bd6a8049-460c-41f8-ae9f-2d347613cc39 33 fields · synced Jun 1, 2026