AccessGUDID - DEVICE: HEDY DENTAL DAM (10686864060311)

GUDID

Device Identifier (DI) Information

Brand Name: HEDY DENTAL DAM
Version or Model: 310DB-5T
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 310DB-5T
Company Name: AMD Medicom Inc

Primary DI Number: 10686864060311
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 52
Labeler D-U-N-S® Number*: 256880576 *Terms of Use

Device Description: HEDY DENTAL DAM - Natural Rubber Latex - 5"x5" - Thin - Blue

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):	Yes
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
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?
11155	Rubber dam, Hevea-latex	A sheet of elastomeric material made of Hevea natural rubber latex (NRL) that is punched with holes and placed over the teeth during dental procedures. It can have a variety of functions such as: 1) to isolate the field of operation from the rest of the oral cavity; 2) to eliminate saliva; 3) to prevent the patient swallowing liquid/dental material; 4) to protect soft tissue from harmful solutions; and 5) to reduce risk of infection. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EIE	DAM, RUBBER

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
Device Size Text, specify: 5 X 5 Inch

Device Record Status

Public Device Record Key: 7a2f95a6-7eea-495a-88b5-fc09e0ad4781
Public Version Date: September 04, 2024
Public Version Number: 1
DI Record Publish Date: August 27, 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: 00686864060314 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: +1(514)636-6262
Email: mkansou@medicom.ca

Phone: +1(514)636-6262 ext: 2309
Email: mdasilva@medicom.ca

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