Device
PUNCH LEFT BACK CUT 100MM
Manufacturer
Bausch & Lomb Incorporated
Model: N2919 L Catalog: N2919 L DI: 00757770508600 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: No Rx: Yes OTC: No
First Published: 2026-04-30 Current Version: 2026-05-08
Description
PUNCH LEFT BACK CUT 100MM
Sterilization
Method Types - Sterilization Method: Moist Heat or Steam Sterilization
Device Sterile: No
Sterilization Prior To Use: Yes
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: e508dfb5-d8db-4387-9ad1-c054cd16e359
Distribution Status: In Commercial Distribution
DUNS Number: 196603781
Device Count: 1
DM Exempt: No
Premarket Exempt: Yes
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: Yes
Serial Number Tracked: No
Manufacturing Date Tracked: No
Expiration Date Tracked: No
Donation ID Number Tracked: No
Labeled Contains NRL: No
Labeled No NRL: No
Identifiers
Device ID: 00757770508600
Type: Primary
Issuing Agency: GS1
GMDN
Code: 33442
Name: Craniofacial rongeur, reusable
Definition:
A hand-held manual surgical instrument with sharp, scoop-shaped jaws designed for cutting tough tissues (cartilage, sinew) or bone, through a cutting/biting action, during surgery involving the cranium and/or face (e.g., craniotomy, ethmoidectomy, mastoidectomy, rhinoplasty); it is not dedicated to dental surgery. It is typically made of metal and designed to withstand the forces required to bite over tough/hard tissue. This is a reusable device.
FDA Product Codes
KAW
Punch, Antrum