Identity
- Trade Name
- Steri-tamp FDA UDI
- Generic Name
- Medicine bottle cap FDA UDI
- Device Name
- 13 mm vial seals Red FDA UDI
- Model / Reference
- ST2103 FDA UDI
- Description
- 13 mm vial seals Red FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00858246002049 FDA UDI
- 510(k) Number
- K974180 FDA UDI
- FDA Product Code
- KPE FDA UDI
- GMDN Term
- Medicine bottle cap FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5025 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Medicine bottle cap
Steri-tamp by Allied Pharmacy Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K974180 also covers:
- Steri-tamp — Allied Pharmacy Products, Inc.
- Steri-tamp — Allied Pharmacy Products, Inc.
- Steri-tamp — Allied Pharmacy Products, Inc.
- Steri-tamp — Allied Pharmacy Products, Inc.
- Steri-tamp — Allied Pharmacy Products, Inc.
- Steri-tamp — Allied Pharmacy Products, Inc.
- Steri-tamp — Allied Pharmacy Products, Inc.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Allied Pharmacy Products, Inc.
Sources (1)
- FDA UDI 32834a78-e8d8-40ba-b0f9-99a7020680e0 34 fields · synced Jun 9, 2026