← Back to catalogue

Ortho Specialties

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
ORTHO SPECIALTIES FDA UDI
Generic Name
Wire ligature FDA UDI
Device Name
Coated Shortie Pre-Twisted Ligature Ties, .012, White (100 ct) FDA UDI
Model / Reference
600-406 FDA UDI
Description
Coated Shortie Pre-Twisted Ligature Ties, .012, White (100 ct) FDA UDI

Identifiers

Catalog Number
600-406 FDA UDI
Primary DI / UDI-DI
00843471143667 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Wire ligature FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Category: Wire ligature

Ortho Specialties by Young Innovations, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire ligature.

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 d39b5aef-a5ec-4f11-94f9-255f22739aad 35 fields · synced May 30, 2026