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Screw Forceps, Self-holding

FDA UDI

Class II (US FDA UDI)

by Double Medical Technology Inc.

Identity

Trade Name
Screw Forceps, Self-holding FDA UDI
Generic Name
Surgical implant handling forceps FDA UDI
Model / Reference
110071400 FDA UDI

Identifiers

Catalog Number
110071400 FDA UDI
Primary DI / UDI-DI
06902139110923 FDA UDI
510(k) Number
K130108 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
GMDN Term
Surgical implant handling forceps FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3040 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 implant handling forceps

Screw Forceps, Self-holding by Double Medical Technology Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant handling forceps.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ed84bd3-38f0-47e0-b0d6-0c60284042c6 35 fields · synced May 31, 2026