ACIER

GUDID 13661522014810

PETERS SURGICAL

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 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 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: 13661522014810
• NIH Device Record Key: 96520b5d-5703-4139-a34a-9ebff2218190
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACIER
• Version Model Number: 31685
• Company DUNS: 265741780
• Company Name: PETERS SURGICAL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03661522014813 [Primary]
GS1	13661522014810 [Package]; Contains: 03661522014813; Package: [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K991073

FDA Product Code

• GAQ: Suture, nonabsorbable, steel, monofilament and multifilament, sterile

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-17
• Device Publish Date: 2020-01-09

On-Brand Devices [ACIER]

• 13661522038885: 31805
• 13661522032586: 3120240
• 13661522028138: 3120245
• 13661522012205: 31803
• 13661522011451: 31766
• 13661522011413: 31802
• 13661522011406: 31801
• 13661522011390: 31800
• 13661522011055: 31600
• 13661522009595: 31765
• 13661522009472: 31764
• 13661522009366: 31846
• 13661522009182: 31845
• 13661522009175: 31763
• 13661522008796: 31681
• 13661522008789: 31680
• 13661522008741: 31762
• 13661522008734: 31842
• 13661522007621: 31761
• 13661522007614: 31760
• 13661522005870: 31N20245
• 13661522005863: 31N20240
• 13661522005849: 31259N20
• 13661522005764: 31720830
• 13661522005757: 31720828
• 13661522005740: 31720827
• 13661522005733: 31720826
• 13661522005726: 31720825
• 13661522005719: 31720824
• 13661522005702: 31720823
• 13661522005696: 31720821
• 13661522043582: 31720831
• 13661522040789: 31509
• 13661522033446: 31804
• 13661522033392: 31640
• 13661522030926: 3120246
• 13661522028664: 31686
• 13661522025243: 31507
• 13661522024123: 31504
• 13661522024116: 31502
• 13661522024109: 31501
• 13661522024093: 317642
• 13661522014810: 31685