AccessGUDID - DEVICE: Symmetry RUMEL (00887482029251)

GUDID

Device Identifier (DI) Information

Brand Name: Symmetry RUMEL
Version or Model: 67-8004
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 67-8004
Company Name: SYMMETRY SURGICAL INC.

Primary DI Number: 00887482029251
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 079641356 *Terms of Use

Device Description: Symmetry® Obturator, Rumel, Child, 6 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:	No
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?
45921	Tracheostomy tube obturator	A device designed to fill the lumen of a tracheostomy tube during its insertion into the stoma created in the larynx (windpipe) to assist in this process, reduce patient trauma, and prevent any tissue damage. When the tracheostomy tube is correctly positioned the obturator is removed. It is typically a thin rod with a bulbous rounded distal end that protrudes out of the tracheostomy tube, and a knob-like handle used to remove it. It is typically made of a high-grade stainless steel and/or silver (Ag) or silver plated brass. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GAH	Stylet, Surgical, General & Plastic Surgery

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: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

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: 30febbe8-1ca1-4e51-9e6e-fbf80c8f5269
Public Version Date: January 17, 2025
Public Version Number: 3
DI Record Publish Date: December 13, 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
No Package DIs found

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

Customer Contact

[?]

No Customer Contact currently defined

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

FDA TOOLS & RESOURCES