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Elmed Incorporated

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED INCORPORATED FDA UDI
Generic Name
Brain spatula FDA UDI
Device Name
Brain Spatulas, Stainless Steel, Ebonized, Malleable, 8”OL (200mm), 3.8mm Tip FDA UDI
Model / Reference
24-0811-SSE FDA UDI
Description
Brain Spatulas, Stainless Steel, Ebonized, Malleable, 8”OL (200mm), 3.8mm Tip FDA UDI

Identifiers

Catalog Number
24-0811-SSE FDA UDI
Primary DI / UDI-DI
00842180166219 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Brain spatula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 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

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Brain spatula

Elmed Incorporated by Elmed Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Brain spatula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 114c0f81-565c-4538-8cbc-7b6025618066 35 fields · synced May 31, 2026