Identity
- Trade Name
- Medline FDA UDI
- Generic Name
- General-purpose endoscopic needle, reusable FDA UDI
- Device Name
- LAP,NEEDLE,IRRIGATING-ASPIRATING,19GAUGE FDA UDI
- Model / Reference
- MDS2231219 FDA UDI
- Description
- LAP,NEEDLE,IRRIGATING-ASPIRATING,19GAUGE FDA UDI
Identifiers
- Catalog Number
- MDS2231219 FDA UDI
- Primary DI / UDI-DI
- 10888277647145 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- General-purpose endoscopic needle, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose endoscopic needle, reusable
Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class I
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class I
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class I
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
- Medline Industries, Inc.
Sources (1)
- FDA UDI f9ea9098-3cdc-474b-89bc-4b8e3e5a3e42 35 fields · synced May 30, 2026