← Back to catalogue

Greenwald Surgical Company, Inc.

FDA UDI

Class II (US FDA UDI)

by Grace Manufacturing Inc

Identity

Trade Name
Greenwald Surgical Company, Inc. FDA UDI
Generic Name
Electrical-only medical device connection cable, reprocessed FDA UDI
Device Name
Cord for Karl Storz #27050 series adult resectoscope. FDA UDI
Model / Reference
77030-01 FDA UDI
Description
Cord for Karl Storz #27050 series adult resectoscope. FDA UDI

Identifiers

Catalog Number
M22 FDA UDI
Primary DI / UDI-DI
10801334005962 FDA UDI
FDA Product Code
FBJ FDA UDI
GMDN Term
Electrical-only medical device connection cable, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 10 Feet FDA UDI

Category: Electrical-only medical device connection cable, reprocessed

Greenwald Surgical Company, Inc. by Grace Manufacturing Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reprocessed.

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
Grace Manufacturing Inc

Sources (1)

  • FDA UDI 8b23d15a-289c-41e0-b5c2-fe2a3c027e5b 35 fields · synced Jun 8, 2026