← Back to catalogue

Slide Hammer

FDA UDI

Class II (US FDA UDI)

by Double Medical Technology Inc.

Identity

Trade Name
Slide Hammer FDA UDI
Generic Name
Surgical mallet FDA UDI
Model / Reference
111193200 FDA UDI

Identifiers

Catalog Number
111193200 FDA UDI
Primary DI / UDI-DI
06902139112019 FDA UDI
510(k) Number
K131609 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Surgical mallet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical mallet

Slide Hammer by Double Medical Technology Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical mallet.

Cleared under the same submission

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

Sources (1)

  • FDA UDI ff9711d5-a5b4-4718-acae-2ee5610ba8d1 35 fields · synced Jun 8, 2026