Identity
- Trade Name
- Shamrock FDA UDI
- Generic Name
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
- Device Name
- Shamrock 30000 Nitrile Examination Powder Free Textured Gloves, Blue, Large FDA UDI
- Model / Reference
- 30313 FDA UDI
- Description
- Shamrock 30000 Nitrile Examination Powder Free Textured Gloves, Blue, Large FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00641932303137 FDA UDI
- 510(k) Number
- K052382 FDA UDI
- FDA Product Code
- LZA FDA UDI
- GMDN Term
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6250 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
Category: Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Shamrock by Shamrock Marketing Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Nitrile examination/treatment glove, non-powdered, non-antimicrobial.
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Cleared under the same submission
K052382 also covers:
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
- Shamrock Marketing Co.
Sources (1)
- FDA UDI bf9ee16a-dc75-43f7-8059-ed2b2d28dac8 34 fields · synced May 30, 2026