AccessGUDID - DEVICE: Symmetry Knolle (00887482107539)

GUDID

Device Identifier (DI) Information

Brand Name: Symmetry Knolle
Version or Model: 60-1183
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 60-1183
Company Name: ASPEN SURGICAL PRODUCTS, INC.

Primary DI Number: 00887482107539
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 027680821 *Terms of Use

Device Description: Symmetry® Cannula, Knolle Anterior Chamber, 30 G, Irrigating

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?
64111	Laparoscopic irrigation cannula	A rigid, hand-operated, single-lumen tube intended to be inserted through a laparoscopic port to provide a conduit for irrigation of body cavities/wounds during a laparoscopic procedure, to facilitate observation. It is not designed to administer parenteral fluids or drugs; it is not designed for surgical aspiration (suction). It is connected via tubing to an appropriate irrigating device (not included). It may be provided with a handle with a valve(s) and hole(s) on its side for the control of irrigation, and/or connection tubing; it is typically made of metal. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HMX	Cannula, Ophthalmic

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: 02383d62-b6f6-49e2-9299-aefd945bb74c
Public Version Date: October 29, 2025
Public Version Number: 3
DI Record Publish Date: August 15, 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: 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

[?]

Phone: +1 888-364-7004
Email: customerservice@symmetrysurgical.com

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