DEVICE: BD SurePath™ Collection Vial Kit 500 (10382904912533)

Device Identifier (DI) Information

BD SurePath™ Collection Vial Kit 500
491253
Not in Commercial Distribution
491253
TRIPATH IMAGING, INC.
10382904912533
GS1
October 18, 2021
25
103318015 *Terms of Use
BD SurePath™ Collection Vial Kit 500: BD SurePath™ Collection Vials (500)
CLOSE

Device Characteristics

Labeling does not contain MRI Safety Information
No
No
Yes
Yes
No
No
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
57952 Cytology specimen container IVD, transport buffer
A covered receptacle containing transport buffer solution intended to be used for the collection, preservation, and transport of a cytology specimen (e.g., oral, cervical, colonic) for in vitro diagnostic investigation [e.g., histopathological cervical cancer screening]. It does not contain patient-contact specimen sampling/extraction devices such as swabs/brushes. This is a single-use device.
Active false
CLOSE

FDA Product Code

[?]
Product Code Product Code Name
MKQ Processor, Cervical Cytology Slide, Automated
CLOSE

FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
P970018 032
No CLOSE

Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
CLOSE

Storage and Handling

[?]
Storage and Handling
Storage Environment Temperature: between 15 and 30 Degrees Celsius
CLOSE

Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
CLOSE

Device Record Status

10a33477-9999-49df-90a7-873db856abb3
October 18, 2021
7
September 08, 2017
CLOSE

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
30382904912537 20 10382904912533 2021-10-18 Not in Commercial Distribution Shelf Pack
CLOSE

Secondary DI

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

Unit of Use DI

[?]
Unit of Use DI Number: 00382904912536 CLOSE

Direct Marking (DM)

[?]
No
No
None
CLOSE

Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
+1(800)638-8663
Technical_Services@bd.com
CLOSE