← Back to catalogue

Clip Gun

FDA UDI

Class II (US FDA UDI)

by Medtronic PS Medical

Identity

Trade Name
Clip Gun FDA UDI
Generic Name
Scalp clip applier, single-use FDA UDI
Device Name
KIT CG8901 CLIP GUN 10 PK FDA UDI
Model / Reference
CG8901 FDA UDI
Description
KIT CG8901 CLIP GUN 10 PK FDA UDI

Identifiers

Primary DI / UDI-DI
20643169109111 FDA UDI
510(k) Number
K050044 FDA UDI
K896723 FDA UDI
FDA Product Code
HBO FDA UDI
GMDN Term
Scalp clip applier, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4150 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Scalp clip applier, single-use

Clip Gun by Medtronic PS Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalp clip applier, single-use.

Cleared under the same submission

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

Sources (1)

  • FDA UDI f4ce0764-41a1-43de-96f8-c8963f10a69a 35 fields · synced May 31, 2026