Ulrich Clamp, Large, Lateral Teeth, 280mm O/L, 87mm Jaw
GUDID 05056405503115
PLATTS & NISBETT LIMITED
Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Primary Device ID | 05056405503115 |
NIH Device Record Key | df9d7b15-dc08-40b6-89df-548cd913519e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ulrich Clamp, Large, Lateral Teeth, 280mm O/L, 87mm Jaw |
Version Model Number | PN0424 |
Company DUNS | 290712512 |
Company Name | PLATTS & NISBETT LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 | false |
OTC Over-The-Counter | false |
Device Identifiers
Device Issuing Agency | Device ID |
---|
GS1 | 05056405503115 [Primary] |
FDA Product Code
Sterilization
Steralize Prior To Use | true |
Device Is Sterile | false |
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
[05056405503115]
Moist Heat or Steam Sterilization
Device Entry Metadata
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-29 |
Device Publish Date | 2023-09-21 |
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