Identity
- Trade Name
- GloShield FDA UDI
- Generic Name
- Laparoscopic access cannula seal, single-use FDA UDI
- Device Name
- GloShield for Olympus Light Cables FDA UDI
- Model / Reference
- 17-2001 FDA UDI
- Description
- GloShield for Olympus Light Cables FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860100001815 FDA UDI
- FDA Product Code
- NWV FDA UDI
- GMDN Term
- Laparoscopic access cannula seal, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.1720 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Laparoscopic access cannula seal, single-use
GloShield by Jackson Medical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Laparoscopic access cannula seal, single-use.
- Convertible Trocar System — APPLIED MEDICAL RESOURCES CORP. · Class II
- Gimmi — Gimmi GmbH · Class II
- Gimmi — Gimmi GmbH · Class II
- Gimmi — Gimmi GmbH · Class II
- Gimmi — Gimmi GmbH · Class II
- Gimmi — Gimmi GmbH · Class II
- Gimmi — Gimmi GmbH · Class II
- Single-Site — Intuitive Surgical, Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Jackson Medical Llc
Sources (1)
- FDA UDI 0c987019-3016-4e16-aa38-bcce33330e0a 34 fields · synced May 30, 2026