AccessGUDID - DEVICE: Machined Medical Litter (AeroSled MA) (00810050862851)

GUDID

Device Identifier (DI) Information

Brand Name: Machined Medical Litter (AeroSled MA)
Version or Model: AS1-061-01
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: LIFEPORT, LLC

Primary DI Number: 00810050862851
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 556196210 *Terms of Use

Device Description: AEROSLED, MACHINED, TD WITH CG PLACARD

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35843	Ambulance stretcher, manual	A manually-operated device consisting of a platform mounted on a wheeled frame designed for use by emergency medical services (EMS) primarily to facilitate easy transport of a recumbent patient to and from ambulance vehicles (e.g., automobiles, aeroplanes, helicopters, boats); it does not include a powered or powered-assisted lifting mechanism. It is typically constructed of lightweight materials and has an undercarriage that opens and folds when it is removed from or pushed into the ambulance; it also usually includes locking devices that match with the locking/docking devices in the ambulance.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FPP	Stretcher, Hand-Carried

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: ec7bfc14-e711-4163-a412-135abd308857
Public Version Date: April 19, 2024
Public Version Number: 1
DI Record Publish Date: April 11, 2024

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: No
Serial Number: Yes
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 360-225-1212
Email: CustomerService@lifeport.com

MENU
- Home
- About
- News
- API
- Download
- Help

FDA TOOLS & RESOURCES