AccessGUDID - DEVICE: HAEMONETICS ORTHOPAT SYSTEM (10812747017046)

GUDID

Device Identifier (DI) Information

Brand Name: HAEMONETICS ORTHOPAT SYSTEM
Version or Model: 01500-00
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: HAEMONETICS CORPORATION

Primary DI Number: 10812747017046
Issuing Agency: GS1
Commercial Distribution End Date: May 09, 2025
Device Count: 1
Labeler D-U-N-S® Number*: 057827420 *Terms of Use

Device Description: ORTHOPAT POST-OP LINE

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:	Yes
Prescription Use (Rx):	Yes
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?
17605	Autotransfusion system blood component processing set	A collection of noninvasive devices that typically includes tubing, containers (e.g., bags or bowls for treatment, reinfusion, waste disposal) and filters intended to be used to process (filter/wash) blood components (e.g., red or white blood cells, platelets) in conjunction with a dedicated pump (not included) as part of an autotransfusion procedure; it is not dedicated to suction and/or anticoagulation. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CAC	Apparatus, Autotransfusion

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K962475	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
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: 89228290-6e61-4dda-bed2-5e650a5992bf
Public Version Date: May 12, 2025
Public Version Number: 6
DI Record Publish Date: June 16, 2017

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
30812747017040	4	20812747017043	2025-05-09	Not in Commercial Distribution	Carton
20812747017043	5	10812747017046	2025-05-09	Not in Commercial Distribution	Dispenser