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Slotted Hammer

FDA UDI

Class I (US FDA UDI)

by I.T.S. GmbH

Identity

Trade Name
Slotted Hammer FDA UDI
Generic Name
Surgical mallet FDA UDI
Device Name
Slotted Hammer FDA UDI
Model / Reference
1UI005A FDA UDI
Description
Slotted Hammer FDA UDI

Identifiers

Catalog Number
1UI005A FDA UDI
Primary DI / UDI-DI
09120116973836 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical mallet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

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: Surgical mallet

Slotted Hammer by I.T.S. GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical mallet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
I.T.S. GmbH

Sources (1)

  • FDA UDI 9a48e939-6fff-4bab-a42f-19882302936b 35 fields · synced Jun 8, 2026