AccessGUDID - DEVICE: Sterling Medical Products (00685404003422)

GUDID

Device Identifier (DI) Information

Brand Name: Sterling Medical Products
Version or Model: 944707
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: APOLLO MEDICAL PRODUCTS CORP.

Primary DI Number: 00685404003422
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 116768422 *Terms of Use

Device Description: HSG TRAY WITH 7FR CATHTER

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):	No
Over the Counter (OTC):	No
Kit:	Yes
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?
37552	Fallopian tube catheterization kit	A collection of sterile devices designed for the transuterine catheterization of the fallopian tubes to inject dye or contrast medium for the evaluation of tubal patency during salpingoscopy/fluoroscopy, ultrasonography, hysteroscopy, or laparoscopy. It typically consists of a dedicated catheter with a balloon, a syringe to inflate the balloon, a secondary catheter [e.g., a tungsten (W) tipped catheter], a guidewire, and connectors. Some types may also facilitate the entry of other devices/instruments for procedures within the fallopian tubes. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
No Product Codes

FDA Premarket Submission

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

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: bd0b7ed8-9f87-44fc-be91-1a2e219d47f2
Public Version Date: June 17, 2024
Public Version Number: 1
DI Record Publish Date: June 07, 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
10685404003429	10	00685404003422		In Commercial Distribution	CARTON

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: Yes
Serial Number: No
Expiration Date: Yes
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 8155375303
Email: jodi@sterlingmedproducts.com

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

FDA TOOLS & RESOURCES