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K-Wire and Steinmann Pin Dispensers

FDA UDI

Class I (US FDA UDI)

by Key Surgical, LLC

Identity

Trade Name
K-Wire and Steinmann Pin Dispensers FDA UDI
Generic Name
Orthopaedic bone pin container FDA UDI
Device Name
K-Wire and Steinmann Pin Dispensers, Dispensing Hole, 18.5-inch Etch w/ 22 FDA UDI
Model / Reference
KI71044 FDA UDI
Description
K-Wire and Steinmann Pin Dispensers, Dispensing Hole, 18.5-inch Etch w/ 22 FDA UDI

Identifiers

Catalog Number
KI71044 FDA UDI
Primary DI / UDI-DI
00849771046363 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Orthopaedic bone pin container 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone pin container

K-Wire and Steinmann Pin Dispensers by Key Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Key Surgical, LLC

Sources (1)

  • FDA UDI 7b2a567f-e3b2-428b-a3e9-879dca775629 35 fields · synced May 30, 2026