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Hexa

FDA UDI

Class I (US FDA UDI)

by Hexa Dental

Identity

Trade Name
Hexa FDA UDI
Generic Name
Scalpel, single-use FDA UDI
Device Name
Hexa Disposable Stainless Steel Scalpels #21 FDA UDI
Model / Reference
PDSS21 FDA UDI
Description
Hexa Disposable Stainless Steel Scalpels #21 FDA UDI

Identifiers

Primary DI / UDI-DI
00850057092066 FDA UDI
FDA Product Code
GDX FDA UDI
GMDN Term
Scalpel, single-use 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

Yes

FDA UDI

Category: Scalpel, single-use

Hexa by Hexa Dental — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalpel, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hexa Dental

Sources (1)

  • FDA UDI c7a08195-df67-405e-8f9e-01003d63d26f 33 fields · synced May 30, 2026