← Back to catalogue

Circular Stapler

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
Circular Stapler FDA UDI
Generic Name
Intraluminal circular stapler, single-use FDA UDI
Model / Reference
FCSLWBE24 FDA UDI

Identifiers

Primary DI / UDI-DI
06939282418552 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Intraluminal circular 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: Intraluminal circular stapler, single-use

Circular 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 Intraluminal circular stapler, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • FDA UDI 977152d7-9d24-49aa-af26-3d293406ad47 32 fields · synced May 30, 2026