AccessGUDID - DEVICE: FABCO (30634303800459)

GUDID

Device Identifier (DI) Information

Brand Name: FABCO
Version or Model: Q606108
Commercial Distribution Status: In Commercial Distribution
Catalog Number: Q606108
Company Name: FIRST AID BANDAGE CO INC

Primary DI Number: 30634303800459
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 001137280 *Terms of Use

Device Description: Femoral Canal Sponge 8 in

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:	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?
47738	Femoral canal sponge	A long, slender, sterile sponge designed to be inserted into the surgically-opened femoral canal to absorb blood and irrigation fluids prior to the insertion of orthopaedic cement and a hip prosthesis. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GDY	Gauze/Sponge, Internal, X-Ray Detectable

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: 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
Height: 20 Millimeter
Width: 28 Millimeter
Length: 20 Centimeter

Device Record Status

Public Device Record Key: 7004982e-e818-4624-b1bf-2b70d190b7cf
Public Version Date: April 05, 2018
Public Version Number: 1
DI Record Publish Date: March 05, 2018

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
50634303800453	5	30634303800459		In Commercial Distribution	Dispenser Box

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: (860) 443-8499
Email: customerservice@fabco.net

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

FDA TOOLS & RESOURCES