ETHI-PAK DS23

GUDID 20705031036731

Stainless Steel, Nonabsorbable Surgical Suture

ETHICON INC.

Metallic suture, monofilament Metallic suture, monofilament Metallic suture, monofilament Metallic suture, monofilament Metallic suture, monofilament Metallic suture, monofilament Metallic suture, monofilament Metallic suture, monofilament Metallic suture, monofilament Metallic suture, monofilament

Primary Device ID	20705031036731
NIH Device Record Key	38a7ca92-62ed-4fc5-8d36-8bee64e41403
Commercial Distribution Status	In Commercial Distribution
Brand Name	ETHI-PAK
Version Model Number	DS23
Catalog Number	DS23
Company DUNS	002144145
Company Name	ETHICON INC.
Device Count	12
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx
Phone	+1(877)384-4266
Email	xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705031036734 [Primary]
GS1	20705031036731 [Package] Contains: 10705031036734 Package: BOX [12 Units] In Commercial Distribution
GS1	80705031036733 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K931271

FDA Product Code

GAQ	SUTURE, NONABSORBABLE, STEEL, MONOFILAMENT AND MULTIFILAMENT, STERILE