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Linear Cutter Stapler

FDA UDI

Class II (US FDA UDI)

by B. J. ZH. F. Panther Medical Equipment Co., Ltd.

Identity

Trade Name
Linear Cutter Stapler FDA UDI
Generic Name
Open-surgery manual linear cutting stapler, single-use FDA UDI
Model / Reference
SSAB-80 4.8 FDA UDI

Identifiers

Primary DI / UDI-DI
06939282466164 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Open-surgery manual linear cutting stapler, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Open-surgery manual linear cutting stapler, single-use

Linear Cutter Stapler by B. J. ZH. F. Panther Medical Equipment Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery manual linear cutting stapler, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 40d4f4ca-d674-4a2c-a3e7-a3245d5c27dd 32 fields · synced May 30, 2026