Identity
- Trade Name
- ELMED FDA UDI
- Generic Name
- Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI
- Device Name
- D’AMICO MEDIASTINOSCOPY FORCEPS, 7 MM WIDTH OVAL CUPPED JAWS CURVED WITHOUT RATCHET, 7MM SHAFT, 11” (28CM) WORKING LENGTH, 15” (38CM) TOTAL LENGTH FDA UDI
- Model / Reference
- 24311-15 FDA UDI
- Description
- D’AMICO MEDIASTINOSCOPY FORCEPS, 7 MM WIDTH OVAL CUPPED JAWS CURVED WITHOUT RATCHET, 7MM SHAFT, 11” (28CM) WORKING LENGTH, 15” (38CM) TOTAL LENGTH FDA UDI
Identifiers
- Catalog Number
- 24311-15 FDA UDI
- Primary DI / UDI-DI
- 00842180156395 FDA UDI
- 510(k) Number
- K181173 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Laparoscopic surgical procedure kit, non-medicated, reusable
Elmed by Elmed Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Laparoscopic surgical procedure kit, non-medicated, reusable.
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class I
- AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
Cleared under the same submission
K181173 also covers:
- Millennium — AVALIGN TECHNOLOGIES, Inc.
- Millennium — AVALIGN TECHNOLOGIES, Inc.
- Millennium — AVALIGN TECHNOLOGIES, Inc.
- Millennium — AVALIGN TECHNOLOGIES, Inc.
- Millennium — AVALIGN TECHNOLOGIES, Inc.
- Millennium — AVALIGN TECHNOLOGIES, Inc.
- Millennium — AVALIGN TECHNOLOGIES, Inc.
- ELMED — ELMED INCORPORATED
- ELMED — ELMED INCORPORATED
- ELMED — ELMED INCORPORATED
- ELMED — ELMED INCORPORATED
- ELMED — ELMED INCORPORATED
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 II | Pending data |
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Manufacturer
- Manufacturer
- Elmed Incorporated
Sources (1)
- FDA UDI fcd3a154-fb06-4e4a-876b-4bac6683b5a2 36 fields · synced May 31, 2026