AccessGUDID - DEVICE: Proximate (10705036013006)

GUDID

Device Identifier (DI) Information

Brand Name: Proximate
Version or Model: PPH03
Commercial Distribution Status: In Commercial Distribution
Catalog Number: PPH03
Company Name: ETHICON ENDO-SURGERY, LLC

Primary DI Number: 10705036013006
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 044606982 *Terms of Use

Device Description: 33mm PROXIMATE PPH, Procedure for Prolapse and Hemorrhoids Set

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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):	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?
46737	Haemorrhoidal surgical stapler, single-use	A sterile, surgical instrument designed to apply surgical staples to tissue in the anal canal to treat haemorrhoids, particularly the procedure for prolapse and haemorrhoids (PPH) [repositioning of the anal canal mucosa to reduce blood flow to internal haemorrhoids]. It is typically pistol-like in design with a rounded, cylindrical head loaded with staples at the distal end, and operating levers at the proximal end intended to deliver a single- or multiple-circular band(s) of staples, whilst cutting away hemorrhoidal tissue. It may include disposable supportive devices intended to assist the procedure (e.g., rectal dilator, anoscope). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GDW	STAPLE, IMPLANTABLE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No 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
No Device Sizes

Device Record Status

Public Device Record Key: d7854626-9b04-4a70-93a1-024b6a02e9da
Public Version Date: October 16, 2019
Public Version Number: 3
DI Record Publish Date: August 24, 2015

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
40705036013007	3	10705036013006		In Commercial Distribution	CASE
20705036013003	3	10705036013006		In Commercial Distribution	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: +1(877)384-4266
Email: customersupport@eesus.jnj.com

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