AccessGUDID - DEVICE: Needle Guide (10841436122877)

GUDID

Device Identifier (DI) Information

Brand Name: Needle Guide
Version or Model: 610-1551
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 610-1551
Company Name: CIVCO MEDICAL INSTRUMENTS CO., INC.

Primary DI Number: 10841436122877
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 134614411 *Terms of Use

Device Description: Sterile TP Pivot Pro™ transperineal needle guide with (2.6x30cm) latex cover

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):	Yes
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?
65809	Percutaneous non-endoscopic instrument access cannula	A hollow slender tubular instrument designed for percutaneous insertion to provide access for instruments (e.g., biopsy needle) under radiological image guidance [e.g., ultrasound] during procedures relating to tissue lesions (e.g., biopsy, ablation). The cannula includes a sharp trocar blade/mandrel to assist introduction and is intended for soft tissue access, however it might additionally be intended for non-impactive bone access. It is not a dedicated bone access cannula and is not an endoscopic (laparoscopic, arthroscopic) access cannula. Some types include a guide/stylet to help percutaneous insertion (e.g., during transperineal prostate biopsy). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IYO	System, imaging, pulsed echo, ultrasonic

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K875236	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Ethylene Oxide

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Keep Away from Sunlight

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 49cd583a-df60-45be-9b87-cbd0c8a19e2a
Public Version Date: March 06, 2025
Public Version Number: 2
DI Record Publish Date: May 03, 2023

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
00841436122870	5	10841436122877		In Commercial Distribution

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: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(319)248-6502
Email: regulatory@civco.com

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