← Back to catalogue

Hermanator Knee Positioning Pad

FDA UDI

Class I (US FDA UDI)

by Aspen Surgical Products, Inc.

Identity

Trade Name
Hermanator Knee Positioning Pad FDA UDI
Generic Name
Orthopaedic knee/leg holder liner FDA UDI
Device Name
Intended to support and maintain the position of an anesthetized patient during surgery FDA UDI
Model / Reference
713100 FDA UDI
Description
Intended to support and maintain the position of an anesthetized patient during surgery FDA UDI

Identifiers

Primary DI / UDI-DI
00840113230815 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Orthopaedic knee/leg holder liner 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: Orthopaedic knee/leg holder liner

Hermanator Knee Positioning Pad by Aspen Surgical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic knee/leg holder liner.

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 df2da067-77cc-4578-b43b-22db7f693760 34 fields · synced Jun 9, 2026