Identity
- Trade Name
- MEDLINE INDUSTRIES, INC. FDA UDI
- Generic Name
- General-purpose syringe, single-use FDA UDI
- Device Name
- SYR W/NDLE,HYPODERM,LL,21GX1.5", 5ML FDA UDI
- Model / Reference
- SYR105217 FDA UDI
- Description
- SYR W/NDLE,HYPODERM,LL,21GX1.5", 5ML FDA UDI
Identifiers
- Catalog Number
- SYR105217 FDA UDI
- Primary DI / UDI-DI
- 10080196449590 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- General-purpose syringe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Weight — 20 Gram FDA UDILength — 1.5 Inch FDA UDI
Category: General-purpose syringe, single-use
Medline Industries, Inc. by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 07e6e4ce-c3ae-4173-941e-90bc9dba40ac 36 fields · synced May 30, 2026