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TRIPOD Stabilizer-Nylon Fastract +2cm

FDA UDI

Class I (US FDA UDI)

by Kdl Medical, Inc.

Identity

Trade Name
TRIPOD Stabilizer-Nylon Fastract +2cm FDA UDI
Generic Name
Patient positioning vacuum pad FDA UDI
Device Name
Heart Stabilizer, Nylon Textured Feet + 2cm FDA UDI
Model / Reference
STB-30C4S-C03 FDA UDI
Description
Heart Stabilizer, Nylon Textured Feet + 2cm FDA UDI

Identifiers

Primary DI / UDI-DI
00899054002456 FDA UDI
FDA Product Code
MWS FDA UDI
GMDN Term
Patient positioning vacuum pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient positioning vacuum pad

TRIPOD Stabilizer-Nylon Fastract +2cm by Kdl Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient positioning vacuum pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kdl Medical, Inc.

Sources (1)

  • FDA UDI 969856dc-0352-4f0a-905c-375f9fd219d7 34 fields · synced Jun 8, 2026