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Sandel

FDA UDI

Class I (US FDA UDI)

by Ansell Sandel Medical Solutions LLC

Identity

Trade Name
SANDEL FDA UDI
Generic Name
Scalpel handle, single-use FDA UDI
Device Name
SANDEL SAFETY SCALPEL HANDLE-LONG, CAB (NS) FDA UDI
Model / Reference
2200-LNS FDA UDI
Description
SANDEL SAFETY SCALPEL HANDLE-LONG, CAB (NS) FDA UDI

Identifiers

Catalog Number
2200-LNS FDA UDI
Primary DI / UDI-DI
25414566810253 FDA UDI
FDA Product Code
GDZ FDA UDI
GMDN Term
Scalpel handle, 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

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

Yes

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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Scalpel handle, single-use

Sandel by Ansell Sandel Medical Solutions LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalpel handle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f73354e9-e34b-476b-b649-1926df6fff44 35 fields · synced Jun 1, 2026