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Clip Deck Assembly

FDA UDI

Class I (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name
Clip Deck Assembly FDA UDI
Generic Name
Ambulance stretcher docking device FDA UDI
Device Name
CLIP DECK ASSEMBLY, 76.00 LONG, STRAIGHT * YELLOW FDA UDI
Model / Reference
100-4033-3-05 FDA UDI
Description
CLIP DECK ASSEMBLY, 76.00 LONG, STRAIGHT * YELLOW FDA UDI

Identifiers

Primary DI / UDI-DI
00810050862981 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Ambulance stretcher docking device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ambulance stretcher docking device

Clip Deck Assembly by Lifeport, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulance stretcher docking device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lifeport, Llc.

Sources (1)

  • FDA UDI 067c21f1-89c8-42fd-aa56-4f79ea861a1f 34 fields · synced May 30, 2026