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MD Traction Rope

FDA UDI

Class I (US FDA UDI)

by Aspen Surgical Products, Inc.

Identity

Trade Name
MD Traction Rope FDA UDI
Generic Name
Traction cord FDA UDI
Device Name
Intended to support and maintain the position of an anesthetized patient during surgery FDA UDI
Model / Reference
715000 FDA UDI
Description
Intended to support and maintain the position of an anesthetized patient during surgery FDA UDI

Identifiers

Primary DI / UDI-DI
00840113230914 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Traction cord FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Traction cord

MD Traction Rope by Aspen Surgical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Traction cord.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca70b3fe-a79c-4f98-8cbd-cd3eb108cfb1 34 fields · synced Jun 9, 2026