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Professional Surgical Instruments Co., Inc.

FDA UDI

Class I (US FDA UDI)

by Professional Surgical Instruments Co., Inc.

Identity

Trade Name
Professional Surgical Instruments Co., Inc. FDA UDI
Generic Name
Airway tube forceps, reusable FDA UDI
Device Name
Adult Magill Forceps with Open Tip FDA UDI
Model / Reference
21-320 FDA UDI
Description
Adult Magill Forceps with Open Tip FDA UDI

Identifiers

Primary DI / UDI-DI
00853863007712 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Airway tube forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Airway tube forceps, reusable

Professional Surgical Instruments Co., Inc. by Professional Surgical Instruments Co., Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Airway tube forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2dad5fc2-a9f8-45c2-a628-2456a93cb92a 33 fields · synced May 30, 2026